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Betamethasone Dipropionate - 54868-5692-0 - (Betamethasone Dipropionate)

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Drug Information of Betamethasone Dipropionate

Product NDC: 54868-5692
Proprietary Name: Betamethasone Dipropionate
Non Proprietary Name: Betamethasone Dipropionate
Active Ingredient(s): .64    mg/g & nbsp;   Betamethasone Dipropionate
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Betamethasone Dipropionate

Product NDC: 54868-5692
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075276
Marketing Category: ANDA
Start Marketing Date: 20061017

Package Information of Betamethasone Dipropionate

Package NDC: 54868-5692-0
Package Description: 15 g in 1 TUBE (54868-5692-0)

NDC Information of Betamethasone Dipropionate

NDC Code 54868-5692-0
Proprietary Name Betamethasone Dipropionate
Package Description 15 g in 1 TUBE (54868-5692-0)
Product NDC 54868-5692
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Betamethasone Dipropionate
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20061017
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name BETAMETHASONE DIPROPIONATE
Strength Number .64
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Betamethasone Dipropionate


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