minoxidil topical solution, 5% (51672-2151)

Drug Facts

Product Profile

Brand Name minoxidil topical solution, 5%

Generic Name minoxidil solution

Labeler sun pharmaceutical industries, inc.

Dosage Form SOLUTION

Routes

TOPICAL

Active Ingredients

minoxidil 50 mg/mL

Manufacturer

Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-2151

Product ID 51672-2151_4c37963d-9845-23d1-e063-6394a90aba45

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA217998

Listing Expiration 2027-12-31

Marketing Start 2025-08-01

Pharmacologic Class

Established (EPC)

arteriolar vasodilator [epc]

Physiologic Effect

arteriolar vasodilation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516722151

Hyphenated Format 51672-2151

Supplemental Identifiers

RxCUI

311724

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 topical solution, 5% (source: ndc)

Generic Name minoxidil solution (source: ndc)

Application Number ANDA217998 (source: ndc)

Routes

TOPICAL

source: ndc

Resolved Composition

Strengths

50 mg/mL

source: ndc

Packaging

1 BOTTLE in 1 CARTON (51672-2151-4) / 60 mL in 1 BOTTLE
3 BOTTLE in 1 CARTON (51672-2151-9) / 60 mL in 1 BOTTLE

source: ndc

Packages (2)

51672-2151-4 1 BOTTLE in 1 CARTON (51672-2151-4) / 60 mL in 1 BOTTLE 51672-2151-9 3 BOTTLE in 1 CARTON (51672-2151-9) / 60 mL in 1 BOTTLE

Ingredients (1)

minoxidil (50 mg/mL)

Linked Drug Pages (1)

Minoxidil Topical Solution, 5% ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["TOPICAL"], "spl_id": "4c37963d-9845-23d1-e063-6394a90aba45", "openfda": {"nui": ["N0000175379", "N0000175564"], "unii": ["5965120SH1"], "rxcui": ["311724"], "spl_set_id": ["acc5ad74-4558-4be9-aab4-94ad9ddad6b2"], "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 BOTTLE in 1 CARTON (51672-2151-4)  / 60 mL in 1 BOTTLE", "package_ndc": "51672-2151-4", "marketing_start_date": "20250801"}, {"sample": false, "description": "3 BOTTLE in 1 CARTON (51672-2151-9)  / 60 mL in 1 BOTTLE", "package_ndc": "51672-2151-9", "marketing_start_date": "20250801"}], "brand_name": "Minoxidil Topical Solution, 5%", "product_id": "51672-2151_4c37963d-9845-23d1-e063-6394a90aba45", "dosage_form": "SOLUTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "51672-2151", "generic_name": "Minoxidil Solution", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Minoxidil Topical Solution, 5%", "active_ingredients": [{"name": "MINOXIDIL", "strength": "50 mg/mL"}], "application_number": "ANDA217998", "marketing_category": "ANDA", "marketing_start_date": "20250801", "listing_expiration_date": "20271231"}