minoxidil for women
Generic: minoxidil
Labeler: sun pharmaceutical industries, inc.Drug Facts
Product Profile
Brand Name
minoxidil for women
Generic Name
minoxidil
Labeler
sun pharmaceutical industries, inc.
Dosage Form
AEROSOL, FOAM
Routes
Active Ingredients
minoxidil 50 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
51672-2129
Product ID
51672-2129_4cb10c82-6bd3-5d62-e063-6394a90afdc9
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA209074
Listing Expiration
2027-12-31
Marketing Start
2019-04-22
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516722129
Hyphenated Format
51672-2129
Supplemental Identifiers
UNII
NUI
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
minoxidil for women (source: ndc)
Generic Name
minoxidil (source: ndc)
Application Number
ANDA209074 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/g
Packaging
- 1 CAN in 1 PACKAGE (51672-2129-4) / 60 g in 1 CAN
- 2 CAN in 1 PACKAGE (51672-2129-8) / 60 g in 1 CAN
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4cb10c82-6bd3-5d62-e063-6394a90afdc9", "openfda": {"nui": ["N0000175379", "N0000175564"], "unii": ["5965120SH1"], "spl_set_id": ["82d7a480-46b2-423b-8da0-a4fc252f7747"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 CAN in 1 PACKAGE (51672-2129-4) / 60 g in 1 CAN", "package_ndc": "51672-2129-4", "marketing_start_date": "20190422"}, {"sample": false, "description": "2 CAN in 1 PACKAGE (51672-2129-8) / 60 g in 1 CAN", "package_ndc": "51672-2129-8", "marketing_start_date": "20190422"}], "brand_name": "Minoxidil For Women", "product_id": "51672-2129_4cb10c82-6bd3-5d62-e063-6394a90afdc9", "dosage_form": "AEROSOL, FOAM", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "51672-2129", "generic_name": "Minoxidil", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Minoxidil", "brand_name_suffix": "For Women", "active_ingredients": [{"name": "MINOXIDIL", "strength": "50 mg/g"}], "application_number": "ANDA209074", "marketing_category": "ANDA", "marketing_start_date": "20190422", "listing_expiration_date": "20271231"}