Tretinoin - 14290-283-20 - (Tretinoin)

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Drug Information of Tretinoin

Product NDC: 14290-283
Proprietary Name: Tretinoin
Non Proprietary Name: Tretinoin
Active Ingredient(s): .25    mg/g & nbsp;   Tretinoin
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Tretinoin

Product NDC: 14290-283
Labeler Name: Triax Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA075264
Marketing Category: NDA
Start Marketing Date: 20090316

Package Information of Tretinoin

Package NDC: 14290-283-20
Package Description: 1 TUBE in 1 CARTON (14290-283-20) > 20 g in 1 TUBE

NDC Information of Tretinoin

NDC Code 14290-283-20
Proprietary Name Tretinoin
Package Description 1 TUBE in 1 CARTON (14290-283-20) > 20 g in 1 TUBE
Product NDC 14290-283
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tretinoin
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20090316
Marketing Category Name NDA
Labeler Name Triax Pharmaceuticals, LLC
Substance Name TRETINOIN
Strength Number .25
Strength Unit mg/g
Pharmaceutical Classes Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of Tretinoin


General Information