Retin-A - 54868-1760-2 - (tretinoin)

Alphabetical Index


Drug Information of Retin-A

Product NDC: 54868-1760
Proprietary Name: Retin-A
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 Retin-A

Product NDC: 54868-1760
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019049
Marketing Category: NDA
Start Marketing Date: 19930528

Package Information of Retin-A

Package NDC: 54868-1760-2
Package Description: 45 g in 1 TUBE (54868-1760-2)

NDC Information of Retin-A

NDC Code 54868-1760-2
Proprietary Name Retin-A
Package Description 45 g in 1 TUBE (54868-1760-2)
Product NDC 54868-1760
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tretinoin
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19930528
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name TRETINOIN
Strength Number .25
Strength Unit mg/g
Pharmaceutical Classes Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of Retin-A


General Information