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Mometasone Furoate - 0781-7068-19 - (Mometasone Furoate)

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Drug Information of Mometasone Furoate

Product NDC: 0781-7068
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: 0781-7068
Labeler Name: Sandoz
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076481
Marketing Category: ANDA
Start Marketing Date: 20031114

Package Information of Mometasone Furoate

Package NDC: 0781-7068-19
Package Description: 45 g in 1 TUBE (0781-7068-19)

NDC Information of Mometasone Furoate

NDC Code 0781-7068-19
Proprietary Name Mometasone Furoate
Package Description 45 g in 1 TUBE (0781-7068-19)
Product NDC 0781-7068
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mometasone Furoate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20031114
Marketing Category Name ANDA
Labeler Name Sandoz
Substance Name MOMETASONE FUROATE
Strength Number 1
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Mometasone Furoate


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