Searching for source:FDA

1,210 results
Record publications over time
Ironsift results are limited for unregistered users. Register or log in to see all records.

US Drug Approval A040259 – FDA – Jul 29, 1999

Hydrocortisone Acetate

1 approved drug product. Hydrocortisone Acetate Ingredients: Hydrocortisone Acetate; Dosage form: cream; Route of administration: topical; Strength: 2.5%; Approval date: July 29, 1999; Marketing status: discontinued.
Full record

US Drug Approval A040267 – FDA – Jul 30, 1998

Butalbital, Acetaminophen and Caffeine

1 approved drug product. Butalbital, Acetaminophen and Caffeine Ingredients: Acetaminophen; Butalbital; Caffeine; Dosage form: tablet; Route of administration: oral; Strength: 500mg;50mg;40mg; Approval date: July 30, 1998; Marketing status: di...
Full record

US Drug Approval A040273 – FDA – Sep 9, 1998

Chloroprocaine Hydrochloride

2 approved drug products. Chloroprocaine Hydrochloride Ingredients: Chloroprocaine Hydrochloride; Dosage form: injectable; Route of administration: injection; Strength: 2%; Approval date: September 9, 1998; Marketing status: prescription. Ch...
Full record

US Drug Approval A040280 – FDA – Sep 30, 1998

Hydrocodone Bitartrate and Acetaminophen

3 approved drug products. Hydrocodone Bitartrate and Acetaminophen Ingredients: Acetaminophen; Hydrocodone Bitartrate; Dosage form: tablet; Route of administration: oral; Strength: 500mg;7.5mg; Approval date: September 30, 1998; Marketing stat...
Full record

US Drug Approval A040286 – FDA – Feb 26, 1999

Leucovorin Calcium Preservative Free

1 approved drug product. Leucovorin Calcium Preservative Free Ingredients: Leucovorin Calcium; Dosage form: injectable; Route of administration: injection; Strength: eq 500mg base/vial; Approval date: February 26, 1999; Marketing status: presc...
Full record

US Drug Approval A040295 – FDA – Dec 1, 2000

Homatropine Methylbromide and Hydrocodone Bitartrate

1 approved drug product. Homatropine Methylbromide and Hydrocodone Bitartrate Ingredients: Homatropine Methylbromide; Hydrocodone Bitartrate; Dosage form: tablet; Route of administration: oral; Strength: 1.5mg;5mg; Approval date: December 1, 20...
Full record

US Drug Approval A040304 – FDA – Oct 2, 2000

Oxycodone and Acetaminophen

1 approved drug product. Oxycodone and Acetaminophen Ingredients: Acetaminophen; Oxycodone Hydrochloride; Dosage form: capsule; Route of administration: oral; Strength: 500mg;5mg; Approval date: October 2, 2000; Marketing status: discontinued....
Full record

US Drug Approval A040308 – FDA – Jul 26, 2000

Hydrocodone Bitartrate and Acetaminophen

2 approved drug products. Hydrocodone Bitartrate and Acetaminophen Ingredients: Acetaminophen; Hydrocodone Bitartrate; Dosage form: tablet; Route of administration: oral; Strength: 500mg;5mg; Approval date: July 26, 2000; Marketing status: dis...
Full record

US Drug Approval A040314 – FDA – Sep 29, 2000

Tropicacyl

1 approved drug product. Tropicacyl Ingredients: Tropicamide; Dosage form: solution/drops; Route of administration: ophthalmic; Strength: 0.5%; Approval date: September 29, 2000; Marketing status: prescription.
Full record

US Drug Approval A040318 – FDA – Oct 5, 1999

Meperidine Hydrochloride

2 approved drug products. Meperidine Hydrochloride Ingredients: Meperidine Hydrochloride; Dosage form: tablet; Route of administration: oral; Strength: 50mg; Approval date: October 5, 1999; Marketing status: discontinued. Meperidine Hydrochl...
Full record

US Drug Approval A040319 – FDA – Sep 7, 1999

Dicyclomine Hydrochloride

1 approved drug product. Dicyclomine Hydrochloride Ingredients: Dicyclomine Hydrochloride; Dosage form: capsule; Route of administration: oral; Strength: 10mg; Approval date: September 7, 1999; Marketing status: prescription.
Full record
Register to view full records and receive email notifications.

US Drug Approval A040327 – FDA – Feb 15, 2000

Orphenadrine Citrate

1 approved drug product. Orphenadrine Citrate Ingredients: Orphenadrine Citrate; Dosage form: tablet, extended release; Route of administration: oral; Strength: 100mg; Approval date: February 15, 2000; Marketing status: prescription.
Full record

US Drug Approval A040330 – FDA – Nov 23, 2001

Percocet

4 approved drug products. Percocet Ingredients: Acetaminophen; Oxycodone Hydrochloride; Dosage form: tablet; Route of administration: oral; Strength: 325mg;2.5mg; Approval date: June 25, 1999; Marketing status: prescription. Percocet Ingre...
Full record

US Drug Approval A040332 – FDA – Jun 28, 1999

Leucovorin Calcium Preservative Free

1 approved drug product. Leucovorin Calcium Preservative Free Ingredients: Leucovorin Calcium; Dosage form: injectable; Route of administration: injection; Strength: eq 10mg base/ml; Approval date: June 28, 1999; Marketing status: discontinued...
Full record

US Drug Approval A040338 – FDA – Jan 31, 2001

Leucovorin Calcium Preservative Free

1 approved drug product. Leucovorin Calcium Preservative Free Ingredients: Leucovorin Calcium; Dosage form: injectable; Route of administration: injection; Strength: eq 50mg base/vial; Approval date: January 31, 2001; Marketing status: discont...
Full record

US Drug Approval A040356 – FDA – May 31, 2000

Hydrocodone Bitartrate and Acetaminophen

1 approved drug product. Hydrocodone Bitartrate and Acetaminophen Ingredients: Acetaminophen; Hydrocodone Bitartrate; Dosage form: tablet; Route of administration: oral; Strength: 500mg;10mg; Approval date: May 31, 2000; Marketing status: disc...
Full record

US Drug Approval A040359 – FDA – Aug 26, 1999

Estropipate

3 approved drug products. Estropipate Ingredients: Estropipate; Dosage form: tablet; Route of administration: oral; Strength: 0.75mg; Approval date: August 26, 1999; Marketing status: prescription. Estropipate Ingredients: Estropipate; Do...
Full record

US Drug Approval A040361 – FDA – Jan 31, 2001

Dextroamphetamine Sulfate

2 approved drug products. Dextroamphetamine Sulfate Ingredients: Dextroamphetamine Sulfate; Dosage form: tablet; Route of administration: oral; Strength: 5mg; Approval date: January 31, 2001; Marketing status: prescription. Dextroamphetamine...
Full record

US Drug Approval A040364 – FDA – Apr 10, 2002

Prednisolone

1 approved drug product. Prednisolone Ingredients: Prednisolone; Dosage form: syrup; Route of administration: oral; Strength: 15mg/5ml; Approval date: April 10, 2002; Marketing status: discontinued.
Full record

US Drug Approval A040366 – FDA – Jan 23, 2002

Hydrocodone Bitartrate and Acetaminophen

1 approved drug product. Hydrocodone Bitartrate and Acetaminophen Ingredients: Acetaminophen; Hydrocodone Bitartrate; Dosage form: solution; Route of administration: oral; Strength: 500mg/15ml;7.5mg/15ml; Approval date: January 23, 2002; Marke...
Full record

US Drug Approval A040367 – FDA – Oct 31, 2002

Dextroamphetamine Sulfate

1 approved drug product. Dextroamphetamine Sulfate Ingredients: Dextroamphetamine Sulfate; Dosage form: tablet; Route of administration: oral; Strength: 10mg; Approval date: October 31, 2002; Marketing status: discontinued.
Full record
Register to view full records and use our APIs.

US Drug Approval A040371 – FDA – Dec 29, 2000

Oxycodone and Acetaminophen

2 approved drug products. Oxycodone and Acetaminophen Ingredients: Acetaminophen; Oxycodone Hydrochloride; Dosage form: tablet; Route of administration: oral; Strength: 500mg;7.5mg; Approval date: December 29, 2000; Marketing status: discontin...
Full record

US Drug Approval A040373 – FDA – Feb 23, 2000

Hydralazine Hydrochloride

1 approved drug product. Hydralazine Hydrochloride Ingredients: Hydralazine Hydrochloride; Dosage form: injectable; Route of administration: injection; Strength: 20mg/ml; Approval date: February 23, 2000; Marketing status: discontinued.
Full record

US Drug Approval A040390 – FDA – Jul 23, 2001

Butalbital, Acetaminophen and Caffeine

1 approved drug product. Butalbital, Acetaminophen and Caffeine Ingredients: Acetaminophen; Butalbital; Caffeine; Dosage form: tablet; Route of administration: oral; Strength: 325mg;50mg;40mg; Approval date: July 23, 2001; Marketing status: di...
Full record

US Drug Approval A040396 – FDA – Feb 27, 2001

Micort-Hc

1 approved drug product. Micort-Hc Ingredients: Hydrocortisone Acetate; Dosage form: cream; Route of administration: topical; Strength: 2.5%; Approval date: February 27, 2001; Marketing status: prescription.
Full record

US Drug Approval A040398 – FDA – Mar 29, 2002

Micort-Hc

1 approved drug product. Micort-Hc Ingredients: Hydrocortisone Acetate; Dosage form: cream; Route of administration: topical; Strength: 2%; Approval date: March 29, 2002; Marketing status: discontinued.
Full record

US Drug Approval A040405 – FDA – Sep 8, 2000

Anexsia 7.5/325

1 approved drug product. Anexsia 7.5/325 Ingredients: Acetaminophen; Hydrocodone Bitartrate; Dosage form: tablet; Route of administration: oral; Strength: 325mg;7.5mg; Approval date: September 8, 2000; Marketing status: prescription.
Full record

US Drug Approval A040407 – FDA – Jul 11, 2001

Prochlorperazine

3 approved drug products. Prochlorperazine Ingredients: Prochlorperazine; Dosage form: suppository; Route of administration: rectal; Strength: 2.5mg; Approval date: July 11, 2001; Marketing status: discontinued. Prochlorperazine Ingredient...
Full record

US Drug Approval A040417 – FDA – Jul 30, 2003

Hydrocortisone

1 approved drug product. Hydrocortisone Ingredients: Hydrocortisone; Dosage form: lotion; Route of administration: topical; Strength: 2.5%; Approval date: July 30, 2003; Marketing status: prescription.
Full record

US Drug Approval A040427 – FDA – Aug 30, 2001

Phentermine Hydrochloride

1 approved drug product. Phentermine Hydrochloride Ingredients: Phentermine Hydrochloride; Dosage form: capsule; Route of administration: oral; Strength: 30mg; Approval date: August 30, 2001; Marketing status: discontinued.
Full record

US Drug Approval A040430 – FDA – Oct 28, 2002

Ethosuximide

1 approved drug product. Ethosuximide Ingredients: Ethosuximide; Dosage form: capsule; Route of administration: oral; Strength: 250mg; Approval date: October 28, 2002; Marketing status: prescription.
Full record
Register to view full records and disable ads.

US Drug Approval A040436 – FDA – Jan 29, 2002

Dextroamphetamine Sulfate

2 approved drug products. Dextroamphetamine Sulfate Ingredients: Dextroamphetamine Sulfate; Dosage form: tablet; Route of administration: oral; Strength: 5mg; Approval date: January 29, 2002; Marketing status: prescription. Dextroamphetamine...
Full record

US Drug Approval A040451 – FDA – Sep 23, 2003

Cyanocobalamin

1 approved drug product. Cyanocobalamin Ingredients: Cyanocobalamin; Dosage form: injectable; Route of administration: injection; Strength: 1mg/ml; Approval date: September 23, 2003; Marketing status: discontinued.
Full record

US Drug Approval A040456 – FDA – May 6, 2003

Dextroamp Saccharate, Amp Aspartate, Dextroamp Sulfate and Amp Sulfate

4 approved drug products. Dextroamp Saccharate, Amp Aspartate, Dextroamp Sulfate and Amp Sulfate Ingredients: Amphetamine Aspartate; Amphetamine Sulfate; Dextroamphetamine Saccharate; Dextroamphetamine Sulfate; Dosage form: tablet; Route of admin...
Full record

US Drug Approval A040461 – FDA – Feb 11, 2004

Mercaptopurine

1 approved drug product. Mercaptopurine Ingredients: Mercaptopurine; Dosage form: tablet; Route of administration: oral; Strength: 50mg; Approval date: February 11, 2004; Marketing status: prescription.
Full record

US Drug Approval A040464 – FDA – Oct 23, 2002

Hydrocodone Bitartrate and Acetaminophen

2 approved drug products. Hydrocodone Bitartrate and Acetaminophen Ingredients: Acetaminophen; Hydrocodone Bitartrate; Dosage form: tablet; Route of administration: oral; Strength: 325mg;7.5mg; Approval date: October 23, 2002; Marketing status...
Full record

US Drug Approval A040466 – FDA – May 28, 2002

Diphenhydramine Hydrochloride

1 approved drug product. Diphenhydramine Hydrochloride Ingredients: Diphenhydramine Hydrochloride; Dosage form: injectable; Route of administration: injection; Strength: 50mg/ml; Approval date: May 28, 2002; Marketing status: prescription.
Full record

US Drug Approval A040467 – FDA – Apr 21, 2003

Triamcinolone Acetonide

2 approved drug products. Triamcinolone Acetonide Ingredients: Triamcinolone Acetonide; Dosage form: lotion; Route of administration: topical; Strength: 0.025%; Approval date: April 21, 2003; Marketing status: prescription. Triamcinolone Ace...
Full record

US Drug Approval A040469 – FDA – Oct 25, 2002

Hydrocodone Bitartrate and Acetaminophen

1 approved drug product. Hydrocodone Bitartrate and Acetaminophen Ingredients: Acetaminophen; Hydrocodone Bitartrate; Dosage form: tablet; Route of administration: oral; Strength: 750mg;7.5mg; Approval date: October 25, 2002; Marketing status:...
Full record

US Drug Approval A040471 – FDA – Nov 21, 2002

Promethazine Hydrochloride

1 approved drug product. Promethazine Hydrochloride Ingredients: Promethazine Hydrochloride; Dosage form: injectable; Route of administration: injection; Strength: 25mg/ml; Approval date: November 21, 2002; Marketing status: discontinued.
Full record

US Drug Approval A040475 – FDA – Apr 28, 2003

Dihydroergotamine Mesylate

1 approved drug product. Dihydroergotamine Mesylate Ingredients: Dihydroergotamine Mesylate; Dosage form: injectable; Route of administration: injection; Strength: 1mg/ml; Approval date: April 28, 2003; Marketing status: prescription.
Full record
Register to view full records and advanced analytics.

US Drug Approval A040477 – FDA – Nov 6, 2002

Hydrocodone Bitartrate and Acetaminophen

1 approved drug product. Hydrocodone Bitartrate and Acetaminophen Ingredients: Acetaminophen; Hydrocodone Bitartrate; Dosage form: tablet; Route of administration: oral; Strength: 500mg;5mg; Approval date: November 6, 2002; Marketing status: d...
Full record

US Drug Approval A040481 – FDA – Aug 21, 2003

Digoxin

1 approved drug product. Digoxin Ingredients: Digoxin; Dosage form: injectable; Route of administration: injection; Strength: 0.25mg/ml; Approval date: August 21, 2003; Marketing status: prescription.
Full record

US Drug Approval A040482 – FDA – Sep 25, 2003

Hydrocodone Bitartrate and Acetaminophen

1 approved drug product. Hydrocodone Bitartrate and Acetaminophen Ingredients: Acetaminophen; Hydrocodone Bitartrate; Dosage form: solution; Route of administration: oral; Strength: 325mg/15ml;7.5mg/15ml; Approval date: September 25, 2003; Mar...
Full record

US Drug Approval A040500 – FDA – Jun 30, 2003

Promethazine Hydrochloride

2 approved drug products. Promethazine Hydrochloride Ingredients: Promethazine Hydrochloride; Dosage form: suppository; Route of administration: rectal; Strength: 12.5mg; Approval date: June 30, 2003; Marketing status: prescription. Prometha...
Full record

US Drug Approval A040507 – FDA – Jul 30, 2003

Propoxyphene Hydrochloride and Acetaminophen

1 approved drug product. Propoxyphene Hydrochloride and Acetaminophen Ingredients: Acetaminophen; Propoxyphene Hydrochloride; Dosage form: tablet; Route of administration: oral; Strength: 650mg;65mg; Approval date: July 30, 2003; Marketing sta...
Full record

US Drug Approval A040514 – FDA – Jun 14, 2005

Folic Acid

1 approved drug product. Folic Acid Ingredients: Folic Acid; Dosage form: tablet; Route of administration: oral; Strength: 1mg; Approval date: June 14, 2005; Marketing status: discontinued.
Full record

US Drug Approval A040522 – FDA – Sep 30, 2004

Norepinephrine Bitartrate

1 approved drug product. Norepinephrine Bitartrate Ingredients: Norepinephrine Bitartrate; Dosage form: injectable; Route of administration: injection; Strength: eq 1mg base/ml; Approval date: September 30, 2004; Marketing status: discontinued...
Full record

US Drug Approval A040530 – FDA – Jan 31, 2005

Testosterone Cypionate

1 approved drug product. Testosterone Cypionate Ingredients: Testosterone Cypionate; Dosage form: injectable; Route of administration: injection; Strength: 200mg/ml; Approval date: January 31, 2005; Marketing status: prescription.
Full record

US Drug Approval A040532 – FDA – Sep 29, 2003

Bethanechol Chloride

1 approved drug product. Bethanechol Chloride Ingredients: Bethanechol Chloride; Dosage form: tablet; Route of administration: oral; Strength: 5mg; Approval date: September 29, 2003; Marketing status: prescription.
Full record