mometasone furoate
Generic: mometasone furoate
Labeler: sun pharmaceutical industries, inc.Drug Facts
Product Profile
Brand Name
mometasone furoate
Generic Name
mometasone furoate
Labeler
sun pharmaceutical industries, inc.
Dosage Form
CREAM
Routes
Active Ingredients
mometasone furoate 1 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
51672-1315
Product ID
51672-1315_3961a44e-34f7-d648-e063-6394a90a974e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076679
Listing Expiration
2026-12-31
Marketing Start
2004-12-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516721315
Hyphenated Format
51672-1315
Supplemental Identifiers
RxCUI
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
ANDA076679 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/g
Packaging
- 1 TUBE in 1 CARTON (51672-1315-1) / 15 g in 1 TUBE
- 1 TUBE in 1 CARTON (51672-1315-6) / 45 g in 1 TUBE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3961a44e-34f7-d648-e063-6394a90a974e", "openfda": {"unii": ["04201GDN4R"], "rxcui": ["311753"], "spl_set_id": ["ce61920d-65df-4423-925d-091e624ea32e"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1315-1) / 15 g in 1 TUBE", "package_ndc": "51672-1315-1", "marketing_start_date": "20041221"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1315-6) / 45 g in 1 TUBE", "package_ndc": "51672-1315-6", "marketing_start_date": "20041221"}], "brand_name": "Mometasone Furoate", "product_id": "51672-1315_3961a44e-34f7-d648-e063-6394a90a974e", "dosage_form": "CREAM", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51672-1315", "generic_name": "Mometasone Furoate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mometasone Furoate", "active_ingredients": [{"name": "MOMETASONE FUROATE", "strength": "1 mg/g"}], "application_number": "ANDA076679", "marketing_category": "ANDA", "marketing_start_date": "20041221", "listing_expiration_date": "20261231"}