Retin-A - 54868-0267-1 - (tretinoin)

Alphabetical Index


Drug Information of Retin-A

Product NDC: 54868-0267
Proprietary Name: Retin-A
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 Retin-A

Product NDC: 54868-0267
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017522
Marketing Category: NDA
Start Marketing Date: 19960101

Package Information of Retin-A

Package NDC: 54868-0267-1
Package Description: 20 g in 1 TUBE (54868-0267-1)

NDC Information of Retin-A

NDC Code 54868-0267-1
Proprietary Name Retin-A
Package Description 20 g in 1 TUBE (54868-0267-1)
Product NDC 54868-0267
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tretinoin
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19960101
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name TRETINOIN
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of Retin-A


General Information