Oralone - 51672-1335-8 - (Triamcinolone Acetonide)

Alphabetical Index


Drug Information of Oralone

Product NDC: 51672-1335
Proprietary Name: Oralone
Non Proprietary Name: Triamcinolone Acetonide
Active Ingredient(s): 1    mg/g & nbsp;   Triamcinolone Acetonide
Administration Route(s): DENTAL
Dosage Form(s): PASTE
Coding System: National Drug Codes(NDC)

Labeler Information of Oralone

Product NDC: 51672-1335
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070730
Marketing Category: ANDA
Start Marketing Date: 19861001

Package Information of Oralone

Package NDC: 51672-1335-8
Package Description: 1 TUBE in 1 CARTON (51672-1335-8) > 7.5 g in 1 TUBE

NDC Information of Oralone

NDC Code 51672-1335-8
Proprietary Name Oralone
Package Description 1 TUBE in 1 CARTON (51672-1335-8) > 7.5 g in 1 TUBE
Product NDC 51672-1335
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Triamcinolone Acetonide
Dosage Form Name PASTE
Route Name DENTAL
Start Marketing Date 19861001
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name TRIAMCINOLONE ACETONIDE
Strength Number 1
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Oralone


General Information