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Betamethasone Dipropionate - 54569-2556-0 - (Betamethasone Dipropionate)

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Drug Information of Betamethasone Dipropionate

Product NDC: 54569-2556
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: 54569-2556
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019137
Marketing Category: NDA
Start Marketing Date: 19840626

Package Information of Betamethasone Dipropionate

Package NDC: 54569-2556-0
Package Description: 1 TUBE in 1 CARTON (54569-2556-0) > 45 g in 1 TUBE

NDC Information of Betamethasone Dipropionate

NDC Code 54569-2556-0
Proprietary Name Betamethasone Dipropionate
Package Description 1 TUBE in 1 CARTON (54569-2556-0) > 45 g in 1 TUBE
Product NDC 54569-2556
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Betamethasone Dipropionate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19840626
Marketing Category Name NDA
Labeler Name A-S Medication Solutions LLC
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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