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Betamethasone Valerate - 0168-0041-60 - (betamethasone valerate)

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Drug Information of Betamethasone Valerate

Product NDC: 0168-0041
Proprietary Name: Betamethasone Valerate
Non Proprietary Name: betamethasone valerate
Active Ingredient(s): 1    mg/mL & nbsp;   betamethasone valerate
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Betamethasone Valerate

Product NDC: 0168-0041
Labeler Name: E. Fougera & Co., a division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018866
Marketing Category: NDA
Start Marketing Date: 19830831

Package Information of Betamethasone Valerate

Package NDC: 0168-0041-60
Package Description: 60 mL in 1 BOTTLE (0168-0041-60)

NDC Information of Betamethasone Valerate

NDC Code 0168-0041-60
Proprietary Name Betamethasone Valerate
Package Description 60 mL in 1 BOTTLE (0168-0041-60)
Product NDC 0168-0041
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name betamethasone valerate
Dosage Form Name LOTION
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/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Betamethasone Valerate


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