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Betamethasone Valerate - 0472-0371-15 - (Betamethasone Valerate)

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Drug Information of Betamethasone Valerate

Product NDC: 0472-0371
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: 0472-0371
Labeler Name: Actavis Mid Atlantic LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070051
Marketing Category: ANDA
Start Marketing Date: 20020901

Package Information of Betamethasone Valerate

Package NDC: 0472-0371-15
Package Description: 1 TUBE in 1 CARTON (0472-0371-15) > 15 g in 1 TUBE

NDC Information of Betamethasone Valerate

NDC Code 0472-0371-15
Proprietary Name Betamethasone Valerate
Package Description 1 TUBE in 1 CARTON (0472-0371-15) > 15 g in 1 TUBE
Product NDC 0472-0371
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 Actavis Mid Atlantic 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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