Home > National Drug Code (NDC) > Mometasone Furoate

Mometasone Furoate - 0713-0701-53 - (Mometasone Furoate)

Alphabetical Index


Drug Information of Mometasone Furoate

Product NDC: 0713-0701
Proprietary Name: Mometasone Furoate
Non Proprietary Name: Mometasone Furoate
Active Ingredient(s): 1    mg/mL & nbsp;   Mometasone Furoate
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Mometasone Furoate

Product NDC: 0713-0701
Labeler Name: GW Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077678
Marketing Category: ANDA
Start Marketing Date: 20071217

Package Information of Mometasone Furoate

Package NDC: 0713-0701-53
Package Description: 60 mL in 1 BOTTLE (0713-0701-53)

NDC Information of Mometasone Furoate

NDC Code 0713-0701-53
Proprietary Name Mometasone Furoate
Package Description 60 mL in 1 BOTTLE (0713-0701-53)
Product NDC 0713-0701
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mometasone Furoate
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 20071217
Marketing Category Name ANDA
Labeler Name GW Laboratories, Inc.
Substance Name MOMETASONE FUROATE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Mometasone Furoate


General Information