TRETIN-X - 63094-0377-2 - (Tretinoin Cream 0.05%)

Alphabetical Index


Drug Information of TRETIN-X

Product NDC: 63094-0377
Proprietary Name: TRETIN-X
Non Proprietary Name: Tretinoin Cream 0.05%
Active Ingredient(s): .5    mg/g & nbsp;   Tretinoin Cream 0.05%
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of TRETIN-X

Product NDC: 63094-0377
Labeler Name: DPT Laboratories, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076498
Marketing Category: ANDA
Start Marketing Date: 20070426

Package Information of TRETIN-X

Package NDC: 63094-0377-2
Package Description: 2 g in 1 TUBE (63094-0377-2)

NDC Information of TRETIN-X

NDC Code 63094-0377-2
Proprietary Name TRETIN-X
Package Description 2 g in 1 TUBE (63094-0377-2)
Product NDC 63094-0377
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tretinoin Cream 0.05%
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20070426
Marketing Category Name ANDA
Labeler Name DPT Laboratories, Ltd.
Substance Name TRETINOIN
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of TRETIN-X


General Information