minoxidil for women

Generic: minoxidil

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minoxidil for women
Generic Name minoxidil
Labeler sun pharmaceutical industries, inc.
Dosage Form AEROSOL, FOAM
Routes
TOPICAL
Active Ingredients

minoxidil 50 mg/g

Manufacturer
Sun Pharmaceutical Industries, Inc.

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)
arteriolar vasodilator [epc]
Physiologic Effect
arteriolar vasodilation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516722129
Hyphenated Format 51672-2129

Supplemental Identifiers

UNII
5965120SH1
NUI
N0000175379 N0000175564

Packaging Origin

Original Packager
true

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
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/g
source: ndc
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
source: ndc

Packages (2)

Ingredients (1)

minoxidil (50 mg/g)

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"}