mometasone furoate
Generic: mometasone furoate
Labeler: glenmark pharmaceuticals inc., usaDrug Facts
Product Profile
Brand Name
mometasone furoate
Generic Name
mometasone furoate
Labeler
glenmark pharmaceuticals inc., usa
Dosage Form
OINTMENT
Routes
Active Ingredients
mometasone furoate 1 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
68462-225
Product ID
68462-225_68dd082e-2bd7-43d5-9dd2-948bd2cd4637
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078571
Listing Expiration
2026-12-31
Marketing Start
2008-05-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68462225
Hyphenated Format
68462-225
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
mometasone furoate (source: ndc)
Generic Name
mometasone furoate (source: ndc)
Application Number
ANDA078571 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/g
Packaging
- 15 g in 1 TUBE (68462-225-17)
- 45 g in 1 TUBE (68462-225-55)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "68dd082e-2bd7-43d5-9dd2-948bd2cd4637", "openfda": {"upc": ["0368462225554"], "unii": ["04201GDN4R"], "rxcui": ["151029"], "spl_set_id": ["209c15dd-72b2-4f00-a2f0-011219f7eaea"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 g in 1 TUBE (68462-225-17)", "package_ndc": "68462-225-17", "marketing_start_date": "20080528"}, {"sample": false, "description": "45 g in 1 TUBE (68462-225-55)", "package_ndc": "68462-225-55", "marketing_start_date": "20080528"}], "brand_name": "Mometasone Furoate", "product_id": "68462-225_68dd082e-2bd7-43d5-9dd2-948bd2cd4637", "dosage_form": "OINTMENT", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68462-225", "generic_name": "Mometasone furoate", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mometasone Furoate", "active_ingredients": [{"name": "MOMETASONE FUROATE", "strength": "1 mg/g"}], "application_number": "ANDA078571", "marketing_category": "ANDA", "marketing_start_date": "20080528", "listing_expiration_date": "20261231"}