Tretinoin - 68682-513-84 - (Tretinoin)

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Drug Information of Tretinoin

Product NDC: 68682-513
Proprietary Name: Tretinoin
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 Tretinoin

Product NDC: 68682-513
Labeler Name: Oceanside Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020475
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20130314

Package Information of Tretinoin

Package NDC: 68682-513-84
Package Description: 1 TUBE in 1 CARTON (68682-513-84) > 45 g in 1 TUBE

NDC Information of Tretinoin

NDC Code 68682-513-84
Proprietary Name Tretinoin
Package Description 1 TUBE in 1 CARTON (68682-513-84) > 45 g in 1 TUBE
Product NDC 68682-513
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tretinoin
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20130314
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Oceanside Pharmaceuticals
Substance Name TRETINOIN
Strength Number .1
Strength Unit mg/g
Pharmaceutical Classes Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of Tretinoin


General Information