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
SOLUTION
Routes
Active Ingredients
mometasone furoate 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51672-1305
Product ID
51672-1305_395e3de6-ccbb-1ae2-e063-6294a90aca6c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076788
Listing Expiration
2026-12-31
Marketing Start
2006-03-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516721305
Hyphenated Format
51672-1305
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
ANDA076788 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (51672-1305-3) / 30 mL in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (51672-1305-4) / 60 mL in 1 BOTTLE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "395e3de6-ccbb-1ae2-e063-6294a90aca6c", "openfda": {"unii": ["04201GDN4R"], "rxcui": ["151030"], "spl_set_id": ["5128842b-99e7-4517-b595-2f3b9cdce086"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (51672-1305-3) / 30 mL in 1 BOTTLE", "package_ndc": "51672-1305-3", "marketing_start_date": "20060315"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (51672-1305-4) / 60 mL in 1 BOTTLE", "package_ndc": "51672-1305-4", "marketing_start_date": "20060315"}], "brand_name": "Mometasone Furoate", "product_id": "51672-1305_395e3de6-ccbb-1ae2-e063-6294a90aca6c", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51672-1305", "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/mL"}], "application_number": "ANDA076788", "marketing_category": "ANDA", "marketing_start_date": "20060315", "listing_expiration_date": "20261231"}