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Mometasone Furoate - 52125-265-01 - (Mometasone Furoate)

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Drug Information of Mometasone Furoate

Product NDC: 52125-265
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): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Mometasone Furoate

Product NDC: 52125-265
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077401
Marketing Category: ANDA
Start Marketing Date: 20130617

Package Information of Mometasone Furoate

Package NDC: 52125-265-01
Package Description: 15 g in 1 TUBE (52125-265-01)

NDC Information of Mometasone Furoate

NDC Code 52125-265-01
Proprietary Name Mometasone Furoate
Package Description 15 g in 1 TUBE (52125-265-01)
Product NDC 52125-265
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mometasone Furoate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20130617
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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