Mometasone Furoate

Product NDC

70518-0175

11-digit product format

705180175

Labeler code

70518

Product ID

70518-0175_9f73046b-ab47-0e99-e053-2a95a90a7e57

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

mometasone furoate

Dosage form

OINTMENT

Route

TOPICAL

Labeler

REMEDYREPACK INC.

Application

ANDA077061

Marketing category

ANDA

Marketing start

2017-01-25

Marketing end

0000-00-00

Substance

MOMETASONE FUROATE

Active strength

1 mg/g

Pharmacologic classes

Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid Hormone Receptor Agonists [MoA]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record