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Alclometasone Dipropionate - 0168-0263-15 - (alclometasone dipropionate)

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Drug Information of Alclometasone Dipropionate

Product NDC: 0168-0263
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: 0168-0263
Labeler Name: E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076973
Marketing Category: ANDA
Start Marketing Date: 20050712

Package Information of Alclometasone Dipropionate

Package NDC: 0168-0263-15
Package Description: 15 g in 1 TUBE (0168-0263-15)

NDC Information of Alclometasone Dipropionate

NDC Code 0168-0263-15
Proprietary Name Alclometasone Dipropionate
Package Description 15 g in 1 TUBE (0168-0263-15)
Product NDC 0168-0263
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name alclometasone dipropionate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20050712
Marketing Category Name ANDA
Labeler Name E. FOUGERA & CO., A division of Fougera Pharmaceuticals 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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