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Alclometasone Dipropionate - 54868-2861-0 - (Alclometasone Dipropionate)

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Drug Information of Alclometasone Dipropionate

Product NDC: 54868-2861
Proprietary Name: Alclometasone Dipropionate
Non Proprietary Name: Alclometasone Dipropionate
Active Ingredient(s): .5    mg/g & nbsp;   Alclometasone Dipropionate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Alclometasone Dipropionate

Product NDC: 54868-2861
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079061
Marketing Category: ANDA
Start Marketing Date: 20090623

Package Information of Alclometasone Dipropionate

Package NDC: 54868-2861-0
Package Description: 1 TUBE in 1 CARTON (54868-2861-0) > 15 g in 1 TUBE

NDC Information of Alclometasone Dipropionate

NDC Code 54868-2861-0
Proprietary Name Alclometasone Dipropionate
Package Description 1 TUBE in 1 CARTON (54868-2861-0) > 15 g in 1 TUBE
Product NDC 54868-2861
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alclometasone Dipropionate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20090623
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name ALCLOMETASONE DIPROPIONATE
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Alclometasone Dipropionate


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