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Betamethasone Dipropionate - 54868-3280-1 - (Betamethasone Dipropionate)

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Drug Information of Betamethasone Dipropionate

Product NDC: 54868-3280
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: 54868-3280
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA019141
Marketing Category: ANDA
Start Marketing Date: 19940427

Package Information of Betamethasone Dipropionate

Package NDC: 54868-3280-1
Package Description: 1 TUBE in 1 CARTON (54868-3280-1) > 15 g in 1 TUBE

NDC Information of Betamethasone Dipropionate

NDC Code 54868-3280-1
Proprietary Name Betamethasone Dipropionate
Package Description 1 TUBE in 1 CARTON (54868-3280-1) > 15 g in 1 TUBE
Product NDC 54868-3280
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Betamethasone Dipropionate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 19940427
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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