Tretinoin - 21695-805-20 - (Tretinoin)

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Drug Information of Tretinoin

Product NDC: 21695-805
Proprietary Name: Tretinoin
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 Tretinoin

Product NDC: 21695-805
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075213
Marketing Category: ANDA
Start Marketing Date: 19981224

Package Information of Tretinoin

Package NDC: 21695-805-20
Package Description: 1 TUBE in 1 CARTON (21695-805-20) > 20 g in 1 TUBE

NDC Information of Tretinoin

NDC Code 21695-805-20
Proprietary Name Tretinoin
Package Description 1 TUBE in 1 CARTON (21695-805-20) > 20 g in 1 TUBE
Product NDC 21695-805
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tretinoin
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19981224
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name TRETINOIN
Strength Number .1
Strength Unit mg/g
Pharmaceutical Classes Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of Tretinoin


General Information