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

Clotrimazole and Betamethasone Dipropionate - 21695-333-45 - (Clotrimazole and Betamethasone Dipropionate)

Alphabetical Index


Drug Information of Clotrimazole and Betamethasone Dipropionate

Product NDC: 21695-333
Proprietary Name: Clotrimazole and Betamethasone Dipropionate
Non Proprietary Name: Clotrimazole and Betamethasone Dipropionate
Active Ingredient(s): .64; 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: 21695-333
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075673
Marketing Category: ANDA
Start Marketing Date: 20010529

Package Information of Clotrimazole and Betamethasone Dipropionate

Package NDC: 21695-333-45
Package Description: 1 TUBE in 1 CARTON (21695-333-45) > 45 g in 1 TUBE

NDC Information of Clotrimazole and Betamethasone Dipropionate

NDC Code 21695-333-45
Proprietary Name Clotrimazole and Betamethasone Dipropionate
Package Description 1 TUBE in 1 CARTON (21695-333-45) > 45 g in 1 TUBE
Product NDC 21695-333
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clotrimazole and Betamethasone Dipropionate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20010529
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE
Strength Number .64; 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