Renova - 0062-0187-04 - (Tretinoin)

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Drug Information of Renova

Product NDC: 0062-0187
Proprietary Name: Renova
Non Proprietary Name: Tretinoin
Active Ingredient(s): .2    mg/g & nbsp;   Tretinoin
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Renova

Product NDC: 0062-0187
Labeler Name: Ortho-McNeil Janssen Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021108
Marketing Category: NDA
Start Marketing Date: 20111018

Package Information of Renova

Package NDC: 0062-0187-04
Package Description: 1 TUBE in 1 CARTON (0062-0187-04) > 2 g in 1 TUBE

NDC Information of Renova

NDC Code 0062-0187-04
Proprietary Name Renova
Package Description 1 TUBE in 1 CARTON (0062-0187-04) > 2 g in 1 TUBE
Product NDC 0062-0187
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tretinoin
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20111018
Marketing Category Name NDA
Labeler Name Ortho-McNeil Janssen Pharmaceuticals, Inc.
Substance Name TRETINOIN
Strength Number .2
Strength Unit mg/g
Pharmaceutical Classes Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of Renova


General Information