Tretinoin - 68788-9834-2 - (tretinoin)

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Drug Information of Tretinoin

Product NDC: 68788-9834
Proprietary Name: Tretinoin
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 Tretinoin

Product NDC: 68788-9834
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075265
Marketing Category: ANDA
Start Marketing Date: 20120329

Package Information of Tretinoin

Package NDC: 68788-9834-2
Package Description: 20 g in 1 TUBE (68788-9834-2)

NDC Information of Tretinoin

NDC Code 68788-9834-2
Proprietary Name Tretinoin
Package Description 20 g in 1 TUBE (68788-9834-2)
Product NDC 68788-9834
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tretinoin
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20120329
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name TRETINOIN
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of Tretinoin


General Information