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Retin-A MICRO - 0062-0190-03 - (Tretinoin)

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Drug Information of Retin-A MICRO

Product NDC: 0062-0190
Proprietary Name: Retin-A MICRO
Non Proprietary Name: Tretinoin
Active Ingredient(s): .1    mg/g & nbsp;   Tretinoin
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Retin-A MICRO

Product NDC: 0062-0190
Labeler Name: Ortho-McNeil Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020475
Marketing Category: NDA
Start Marketing Date: 20110501

Package Information of Retin-A MICRO

Package NDC: 0062-0190-03
Package Description: 1 TUBE in 1 CARTON (0062-0190-03) > 45 g in 1 TUBE

NDC Information of Retin-A MICRO

NDC Code 0062-0190-03
Proprietary Name Retin-A MICRO
Package Description 1 TUBE in 1 CARTON (0062-0190-03) > 45 g in 1 TUBE
Product NDC 0062-0190
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tretinoin
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20110501
Marketing Category Name NDA
Labeler Name Ortho-McNeil Pharmaceuticals
Substance Name TRETINOIN
Strength Number .1
Strength Unit mg/g
Pharmaceutical Classes Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of Retin-A MICRO


General Information