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Betamethasone Valerate - 21695-584-15 - (Betamethasone Valerate)

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Drug Information of Betamethasone Valerate

Product NDC: 21695-584
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: 21695-584
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070062
Marketing Category: ANDA
Start Marketing Date: 19850514

Package Information of Betamethasone Valerate

Package NDC: 21695-584-15
Package Description: 1 TUBE in 1 CARTON (21695-584-15) > 15 g in 1 TUBE

NDC Information of Betamethasone Valerate

NDC Code 21695-584-15
Proprietary Name Betamethasone Valerate
Package Description 1 TUBE in 1 CARTON (21695-584-15) > 15 g in 1 TUBE
Product NDC 21695-584
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Betamethasone Valerate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19850514
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
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


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