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Betamethasone Valerate - 54569-0793-0 - (Betamethasone Valerate)

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Drug Information of Betamethasone Valerate

Product NDC: 54569-0793
Proprietary Name: Betamethasone Valerate
Non Proprietary Name: Betamethasone Valerate
Active Ingredient(s): 1.2    mg/g & nbsp;   Betamethasone Valerate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Betamethasone Valerate

Product NDC: 54569-0793
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070051
Marketing Category: ANDA
Start Marketing Date: 20020901

Package Information of Betamethasone Valerate

Package NDC: 54569-0793-0
Package Description: 1 TUBE in 1 CARTON (54569-0793-0) > 15 g in 1 TUBE

NDC Information of Betamethasone Valerate

NDC Code 54569-0793-0
Proprietary Name Betamethasone Valerate
Package Description 1 TUBE in 1 CARTON (54569-0793-0) > 15 g in 1 TUBE
Product NDC 54569-0793
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Betamethasone Valerate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20020901
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions LLC
Substance Name BETAMETHASONE VALERATE
Strength Number 1.2
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Betamethasone Valerate


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