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Betamethasone Dipropionate - 52959-721-45 - (Betamethasone Dipropionate)

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Drug Information of Betamethasone Dipropionate

Product NDC: 52959-721
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
Coding System: National Drug Codes(NDC)

Labeler Information of Betamethasone Dipropionate

Product NDC: 52959-721
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA019137
Marketing Category: ANDA
Start Marketing Date: 19840226

Package Information of Betamethasone Dipropionate

Package NDC: 52959-721-45
Package Description: 45 g in 1 TUBE (52959-721-45)

NDC Information of Betamethasone Dipropionate

NDC Code 52959-721-45
Proprietary Name Betamethasone Dipropionate
Package Description 45 g in 1 TUBE (52959-721-45)
Product NDC 52959-721
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Betamethasone Dipropionate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19840226
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, 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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