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Betamethasone Dipropionate - 0168-0267-30 - (Betamethasone Dipropionate)

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Drug Information of Betamethasone Dipropionate

Product NDC: 0168-0267
Proprietary Name: Betamethasone Dipropionate
Non Proprietary Name: Betamethasone Dipropionate
Active Ingredient(s): .5    mg/mL & nbsp;   Betamethasone Dipropionate
Administration Route(s): TOPICAL
Dosage Form(s): LOTION, AUGMENTED
Coding System: National Drug Codes(NDC)

Labeler Information of Betamethasone Dipropionate

Product NDC: 0168-0267
Labeler Name: E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077111
Marketing Category: ANDA
Start Marketing Date: 20070521

Package Information of Betamethasone Dipropionate

Package NDC: 0168-0267-30
Package Description: 30 mL in 1 BOTTLE (0168-0267-30)

NDC Information of Betamethasone Dipropionate

NDC Code 0168-0267-30
Proprietary Name Betamethasone Dipropionate
Package Description 30 mL in 1 BOTTLE (0168-0267-30)
Product NDC 0168-0267
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Betamethasone Dipropionate
Dosage Form Name LOTION, AUGMENTED
Route Name TOPICAL
Start Marketing Date 20070521
Marketing Category Name ANDA
Labeler Name E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.
Substance Name BETAMETHASONE DIPROPIONATE
Strength Number .5
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Betamethasone Dipropionate


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