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
OINTMENT
Routes
Active Ingredients
mometasone furoate 1 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
51672-1311
Product ID
51672-1311_39619c2c-5804-85d9-e063-6294a90aa109
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076624
Listing Expiration
2026-12-31
Marketing Start
2004-12-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516721311
Hyphenated Format
51672-1311
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
ANDA076624 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/g
Packaging
- 1 TUBE in 1 CARTON (51672-1311-1) / 15 g in 1 TUBE
- 1 TUBE in 1 CARTON (51672-1311-6) / 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": "39619c2c-5804-85d9-e063-6294a90aa109", "openfda": {"unii": ["04201GDN4R"], "rxcui": ["151029"], "spl_set_id": ["d8cf50d4-0448-4527-a498-cddd511213f0"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1311-1) / 15 g in 1 TUBE", "package_ndc": "51672-1311-1", "marketing_start_date": "20041203"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1311-6) / 45 g in 1 TUBE", "package_ndc": "51672-1311-6", "marketing_start_date": "20041203"}], "brand_name": "Mometasone Furoate", "product_id": "51672-1311_39619c2c-5804-85d9-e063-6294a90aa109", "dosage_form": "OINTMENT", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51672-1311", "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": "ANDA076624", "marketing_category": "ANDA", "marketing_start_date": "20041203", "listing_expiration_date": "20261231"}