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Betamethasone Dipropionate - 51672-1310-3 - (Betamethasone Dipropionate)

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Drug Information of Betamethasone Dipropionate

Product NDC: 51672-1310
Proprietary Name: Betamethasone Dipropionate
Non Proprietary Name: Betamethasone Dipropionate
Active Ingredient(s): .5    mg/g & nbsp;   Betamethasone Dipropionate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM, AUGMENTED
Coding System: National Drug Codes(NDC)

Labeler Information of Betamethasone Dipropionate

Product NDC: 51672-1310
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076543
Marketing Category: ANDA
Start Marketing Date: 20031209

Package Information of Betamethasone Dipropionate

Package NDC: 51672-1310-3
Package Description: 1 TUBE in 1 CARTON (51672-1310-3) > 50 g in 1 TUBE

NDC Information of Betamethasone Dipropionate

NDC Code 51672-1310-3
Proprietary Name Betamethasone Dipropionate
Package Description 1 TUBE in 1 CARTON (51672-1310-3) > 50 g in 1 TUBE
Product NDC 51672-1310
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Betamethasone Dipropionate
Dosage Form Name CREAM, AUGMENTED
Route Name TOPICAL
Start Marketing Date 20031209
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name BETAMETHASONE DIPROPIONATE
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Betamethasone Dipropionate


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