TRETIN.X - 16781-376-35 - (TRETINOIN)

Alphabetical Index


Drug Information of TRETIN.X

Product NDC: 16781-376
Proprietary Name: TRETIN.X
Non Proprietary Name: TRETINOIN
Active Ingredient(s): .375    mg/g & nbsp;   TRETINOIN
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of TRETIN.X

Product NDC: 16781-376
Labeler Name: Onset Dermatologics LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090098
Marketing Category: ANDA
Start Marketing Date: 20130402

Package Information of TRETIN.X

Package NDC: 16781-376-35
Package Description: 1 TUBE in 1 CARTON (16781-376-35) > 35 g in 1 TUBE

NDC Information of TRETIN.X

NDC Code 16781-376-35
Proprietary Name TRETIN.X
Package Description 1 TUBE in 1 CARTON (16781-376-35) > 35 g in 1 TUBE
Product NDC 16781-376
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TRETINOIN
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20130402
Marketing Category Name ANDA
Labeler Name Onset Dermatologics LLC
Substance Name TRETINOIN
Strength Number .375
Strength Unit mg/g
Pharmaceutical Classes Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of TRETIN.X


General Information