Retin-A - 0062-0275-23 - (Tretinoin)

Alphabetical Index


Drug Information of Retin-A

Product NDC: 0062-0275
Proprietary Name: Retin-A
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 Retin-A

Product NDC: 0062-0275
Labeler Name: Ortho-McNeil Janssen Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017340
Marketing Category: NDA
Start Marketing Date: 19730430

Package Information of Retin-A

Package NDC: 0062-0275-23
Package Description: 1 TUBE in 1 CARTON (0062-0275-23) > 20 g in 1 TUBE

NDC Information of Retin-A

NDC Code 0062-0275-23
Proprietary Name Retin-A
Package Description 1 TUBE in 1 CARTON (0062-0275-23) > 20 g in 1 TUBE
Product NDC 0062-0275
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tretinoin
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19730430
Marketing Category Name NDA
Labeler Name Ortho-McNeil Janssen Pharmaceuticals, Inc.
Substance Name TRETINOIN
Strength Number 1
Strength Unit mg/g
Pharmaceutical Classes Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of Retin-A


General Information