Mometasone Furoate

Basic Information

Product Name

Mometasone Furoate

FDA Product Code

63629-9306

Regulatory Information

NDC Product Code

63629-9306

Application Number

ANDA076067

Marketing Category

C73584

Effective Date

July 7, 2022

Territorial Authority

USA

FDA Title

These highlights do not include all the information needed to use safely and effectively. See full prescribing information for .MOMETASONE FUROATE ointment, for topical useInitial U.S. Approval: 1987

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Version Number

101

Active Ingredients

MOMETASONE FUROATE

Quantity: 1 mg in 1 g

Code: 04201GDN4R

Class Code: ACTIB

HEXYLENE GLYCOL

Code: KEH0A3F75J

Class Code: IACT

PROPYLENE GLYCOL MONOSTEARATE

Code: MZM1I680W0

Class Code: IACT

PETROLATUM

Code: 4T6H12BN9U

Class Code: IACT

WHITE WAX

Code: 7G1J5DA97F

Class Code: IACT

PHOSPHORIC ACID

Code: E4GA8884NN

Class Code: IACT

WATER

Code: 059QF0KO0R

Class Code: IACT

Active Moieties

MOMETASONE

Code: 8HR4QJ6DW8

Basic Information

Regulatory Information

Company Information

Active Ingredients

HEXYLENE GLYCOL

PROPYLENE GLYCOL MONOSTEARATE

PETROLATUM

WHITE WAX

PHOSPHORIC ACID

WATER

Active Moieties

MOMETASONE