Tretinoin - 54868-4379-0 - (Tretinoin)

Alphabetical Index


Drug Information of Tretinoin

Product NDC: 54868-4379
Proprietary Name: Tretinoin
Non Proprietary Name: Tretinoin
Active Ingredient(s): .1    mg/g & nbsp;   Tretinoin
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Tretinoin

Product NDC: 54868-4379
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA017340
Marketing Category: ANDA
Start Marketing Date: 20081017

Package Information of Tretinoin

Package NDC: 54868-4379-0
Package Description: 1 TUBE in 1 CARTON (54868-4379-0) > 45 g in 1 TUBE

NDC Information of Tretinoin

NDC Code 54868-4379-0
Proprietary Name Tretinoin
Package Description 1 TUBE in 1 CARTON (54868-4379-0) > 45 g in 1 TUBE
Product NDC 54868-4379
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tretinoin
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20081017
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name TRETINOIN
Strength Number .1
Strength Unit mg/g
Pharmaceutical Classes Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of Tretinoin


General Information