Mometasone Furoate

Product NDC
68071-1538
11-digit product format
680711538
Labeler code
68071
Product ID
68071-1538_bb11f91c-b47b-e758-e053-2995a90afdc5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Mometasone Furoate
Dosage form
CREAM
Route
TOPICAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA078541
Marketing category
ANDA
Marketing start
2008-05-28
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
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68071-1538-56807115380545 g in 1 BOX (68071-1538-5) 45 g2017-07-250000-00-00NoNoCurrent