Tretin-X - 14290-377-35 - (tretinoin)

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Drug Information of Tretin-X

Product NDC: 14290-377
Proprietary Name: Tretin-X
Non Proprietary Name: tretinoin
Active Ingredient(s): .5    mg/g & nbsp;   tretinoin
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Tretin-X

Product NDC: 14290-377
Labeler Name: Triax Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075265
Marketing Category: ANDA
Start Marketing Date: 20100801

Package Information of Tretin-X

Package NDC: 14290-377-35
Package Description: 1 TUBE in 1 CARTON (14290-377-35) > 35 g in 1 TUBE

NDC Information of Tretin-X

NDC Code 14290-377-35
Proprietary Name Tretin-X
Package Description 1 TUBE in 1 CARTON (14290-377-35) > 35 g in 1 TUBE
Product NDC 14290-377
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tretinoin
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20100801
Marketing Category Name ANDA
Labeler Name Triax Pharmaceuticals, LLC
Substance Name TRETINOIN
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of Tretin-X


General Information