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Mometasone Furoate - 0115-1471-54 - (Mometasone Furoate)

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Drug Information of Mometasone Furoate

Product NDC: 0115-1471
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): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Mometasone Furoate

Product NDC: 0115-1471
Labeler Name: Global Pharmaceuticals, Division of Impax Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076499
Marketing Category: ANDA
Start Marketing Date: 20071121

Package Information of Mometasone Furoate

Package NDC: 0115-1471-54
Package Description: 1 BOTTLE in 1 CARTON (0115-1471-54) > 27.5 g in 1 BOTTLE

NDC Information of Mometasone Furoate

NDC Code 0115-1471-54
Proprietary Name Mometasone Furoate
Package Description 1 BOTTLE in 1 CARTON (0115-1471-54) > 27.5 g in 1 BOTTLE
Product NDC 0115-1471
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mometasone Furoate
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20071121
Marketing Category Name ANDA
Labeler Name Global Pharmaceuticals, Division of Impax Laboratories Inc.
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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