Home > National Drug Code (NDC) > BETAMETHASONE VALERATE

BETAMETHASONE VALERATE - 54569-1115-0 - (Betamethasone Valerate)

Alphabetical Index


Drug Information of BETAMETHASONE VALERATE

Product NDC: 54569-1115
Proprietary Name: BETAMETHASONE VALERATE
Non Proprietary Name: Betamethasone Valerate
Active Ingredient(s): 1    mg/g & nbsp;   Betamethasone Valerate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of BETAMETHASONE VALERATE

Product NDC: 54569-1115
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072041
Marketing Category: ANDA
Start Marketing Date: 19880106

Package Information of BETAMETHASONE VALERATE

Package NDC: 54569-1115-0
Package Description: 1 TUBE in 1 CARTON (54569-1115-0) > 15 g in 1 TUBE

NDC Information of BETAMETHASONE VALERATE

NDC Code 54569-1115-0
Proprietary Name BETAMETHASONE VALERATE
Package Description 1 TUBE in 1 CARTON (54569-1115-0) > 15 g in 1 TUBE
Product NDC 54569-1115
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Betamethasone Valerate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19880106
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions LLC
Substance Name BETAMETHASONE VALERATE
Strength Number 1
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of BETAMETHASONE VALERATE


General Information