minoxidil 5% (for men)

Generic: minoxidil

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

Drug Facts

Product Profile

Brand Name minoxidil 5% (for men)
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 51672-2128
Product ID 51672-2128_4cb0e64f-2d3a-bde3-e063-6294a90a769f
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA209074
Listing Expiration 2027-12-31
Marketing Start 2019-01-02

Pharmacologic Class

Established (EPC)
arteriolar vasodilator [epc]
Physiologic Effect
arteriolar vasodilation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516722128
Hyphenated Format 51672-2128

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 5% (for men) (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 (51672-2128-4) / 60 g in 1 CAN
  • 3 CAN in 1 PACKAGE (51672-2128-9) / 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": "4cb0e64f-2d3a-bde3-e063-6294a90a769f", "openfda": {"nui": ["N0000175379", "N0000175564"], "unii": ["5965120SH1"], "spl_set_id": ["52210e2d-d87c-4b53-9b58-95c65c9d11fa"], "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 (51672-2128-4)  / 60 g in 1 CAN", "package_ndc": "51672-2128-4", "marketing_start_date": "20190102"}, {"sample": false, "description": "3 CAN in 1 PACKAGE (51672-2128-9)  / 60 g in 1 CAN", "package_ndc": "51672-2128-9", "marketing_start_date": "20190102"}], "brand_name": "Minoxidil 5% (For Men)", "product_id": "51672-2128_4cb0e64f-2d3a-bde3-e063-6294a90a769f", "dosage_form": "AEROSOL, FOAM", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "51672-2128", "generic_name": "Minoxidil", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Minoxidil", "brand_name_suffix": "5% (For Men)", "active_ingredients": [{"name": "MINOXIDIL", "strength": "50 mg/g"}], "application_number": "ANDA209074", "marketing_category": "ANDA", "marketing_start_date": "20190102", "listing_expiration_date": "20271231"}