Home > National Drug Code (NDC) > Clotrimazole and Betamethasone Dipropionate

Clotrimazole and Betamethasone Dipropionate - 0472-0379-45 - (Clotrimazole and Betamethasone Dipropionate)

Alphabetical Index


Drug Information of Clotrimazole and Betamethasone Dipropionate

Product NDC: 0472-0379
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: 0472-0379
Labeler Name: Actavis Mid Atlantic LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076002
Marketing Category: ANDA
Start Marketing Date: 20070103

Package Information of Clotrimazole and Betamethasone Dipropionate

Package NDC: 0472-0379-45
Package Description: 1 TUBE in 1 CARTON (0472-0379-45) > 45 g in 1 TUBE

NDC Information of Clotrimazole and Betamethasone Dipropionate

NDC Code 0472-0379-45
Proprietary Name Clotrimazole and Betamethasone Dipropionate
Package Description 1 TUBE in 1 CARTON (0472-0379-45) > 45 g in 1 TUBE
Product NDC 0472-0379
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clotrimazole and Betamethasone Dipropionate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20070103
Marketing Category Name ANDA
Labeler Name Actavis Mid Atlantic LLC
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


General Information