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Betamethasone Dipropionate - 68788-0972-4 - (Betamethasone Dipropionate)

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Drug Information of Betamethasone Dipropionate

Product NDC: 68788-0972
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: 68788-0972
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071012
Marketing Category: ANDA
Start Marketing Date: 19870203

Package Information of Betamethasone Dipropionate

Package NDC: 68788-0972-4
Package Description: 45 g in 1 TUBE (68788-0972-4)

NDC Information of Betamethasone Dipropionate

NDC Code 68788-0972-4
Proprietary Name Betamethasone Dipropionate
Package Description 45 g in 1 TUBE (68788-0972-4)
Product NDC 68788-0972
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Betamethasone Dipropionate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 19870203
Marketing Category Name ANDA
Labeler Name Preferred 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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