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Mometasone Furoate - 68462-192-17 - (Mometasone Furoate)

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Drug Information of Mometasone Furoate

Product NDC: 68462-192
Proprietary Name: Mometasone Furoate
Non Proprietary Name: Mometasone Furoate
Active Ingredient(s): 1    mg/g & nbsp;   Mometasone Furoate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Mometasone Furoate

Product NDC: 68462-192
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078541
Marketing Category: ANDA
Start Marketing Date: 20080528

Package Information of Mometasone Furoate

Package NDC: 68462-192-17
Package Description: 15 g in 1 TUBE (68462-192-17)

NDC Information of Mometasone Furoate

NDC Code 68462-192-17
Proprietary Name Mometasone Furoate
Package Description 15 g in 1 TUBE (68462-192-17)
Product NDC 68462-192
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mometasone Furoate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20080528
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc., USA
Substance Name MOMETASONE FUROATE
Strength Number 1
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Mometasone Furoate


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