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Betamethasone Valerate - 0168-0040-46 - (betamethasone valerate)

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Drug Information of Betamethasone Valerate

Product NDC: 0168-0040
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: 0168-0040
Labeler Name: E. Fougera & Co., a division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018861
Marketing Category: NDA
Start Marketing Date: 19830831

Package Information of Betamethasone Valerate

Package NDC: 0168-0040-46
Package Description: 45 g in 1 TUBE (0168-0040-46)

NDC Information of Betamethasone Valerate

NDC Code 0168-0040-46
Proprietary Name Betamethasone Valerate
Package Description 45 g in 1 TUBE (0168-0040-46)
Product NDC 0168-0040
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name betamethasone valerate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19830831
Marketing Category Name NDA
Labeler Name E. Fougera & Co., a division of Fougera Pharmaceuticals Inc.
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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