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Clotrimazole and Betamethasone Dipropionate - 0168-0258-46 - (Clotrimazole and Betamethasone Dipropionate)

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Drug Information of Clotrimazole and Betamethasone Dipropionate

Product NDC: 0168-0258
Proprietary Name: Clotrimazole and Betamethasone Dipropionate
Non Proprietary Name: Clotrimazole and Betamethasone Dipropionate
Active Ingredient(s): .5; 10    mg/g; mg/g & nbsp;   Clotrimazole and Betamethasone Dipropionate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Clotrimazole and Betamethasone Dipropionate

Product NDC: 0168-0258
Labeler Name: E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075502
Marketing Category: ANDA
Start Marketing Date: 20010605

Package Information of Clotrimazole and Betamethasone Dipropionate

Package NDC: 0168-0258-46
Package Description: 45 g in 1 TUBE (0168-0258-46)

NDC Information of Clotrimazole and Betamethasone Dipropionate

NDC Code 0168-0258-46
Proprietary Name Clotrimazole and Betamethasone Dipropionate
Package Description 45 g in 1 TUBE (0168-0258-46)
Product NDC 0168-0258
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clotrimazole and Betamethasone Dipropionate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20010605
Marketing Category Name ANDA
Labeler Name E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc.
Substance Name BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE
Strength Number .5; 10
Strength Unit mg/g; mg/g
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Clotrimazole and Betamethasone Dipropionate


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