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Betamethasone Dipropionate - 0168-0056-15 - (Betamethasone Dipropionate)

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Drug Information of Betamethasone Dipropionate

Product NDC: 0168-0056
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): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Betamethasone Dipropionate

Product NDC: 0168-0056
Labeler Name: E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019141
Marketing Category: NDA
Start Marketing Date: 19840904

Package Information of Betamethasone Dipropionate

Package NDC: 0168-0056-15
Package Description: 1 TUBE in 1 CARTON (0168-0056-15) > 15 g in 1 TUBE

NDC Information of Betamethasone Dipropionate

NDC Code 0168-0056-15
Proprietary Name Betamethasone Dipropionate
Package Description 1 TUBE in 1 CARTON (0168-0056-15) > 15 g in 1 TUBE
Product NDC 0168-0056
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Betamethasone Dipropionate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 19840904
Marketing Category Name NDA
Labeler Name E. Fougera & Co. a division of Fougera Pharmaceuticals 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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