minoxidil topical solution 2%

Generic: minoxidil topical solution 2%

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

Drug Facts

Product Profile

Brand Name minoxidil topical solution 2%
Generic Name minoxidil topical solution 2%
Labeler sun pharmaceutical industries, inc.
Dosage Form SOLUTION
Routes
TOPICAL
Active Ingredients

minoxidil 20 mg/mL

Manufacturer
SUN PHARMACEUTICAL INDUSTRIES, INC.

Identifiers & Regulatory

Product NDC 51672-2152
Product ID 51672-2152_4c3823f2-ce4b-afea-e063-6294a90a03c0
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA218175
Listing Expiration 2027-12-31
Marketing Start 2025-09-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516722152
Hyphenated Format 51672-2152

Supplemental Identifiers

RxCUI
311723
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 2% (source: ndc)
Generic Name minoxidil topical solution 2% (source: ndc)
Application Number ANDA218175 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (51672-2152-4) / 60 mL in 1 BOTTLE
  • 3 BOTTLE in 1 CARTON (51672-2152-9) / 60 mL in 1 BOTTLE
source: ndc

Packages (2)

51672-2152-4 1 BOTTLE in 1 CARTON (51672-2152-4) / 60 mL in 1 BOTTLE 51672-2152-9 3 BOTTLE in 1 CARTON (51672-2152-9) / 60 mL in 1 BOTTLE

Ingredients (1)

minoxidil (20 mg/mL)

Linked Drug Pages (1)

Minoxidil Topical Solution 2% ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4c3823f2-ce4b-afea-e063-6294a90a03c0", "openfda": {"nui": ["N0000175379", "N0000175564"], "unii": ["5965120SH1"], "rxcui": ["311723"], "spl_set_id": ["15d7cdd7-6d37-477c-bce7-a459ea960a53"], "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 (51672-2152-4)  / 60 mL in 1 BOTTLE", "package_ndc": "51672-2152-4", "marketing_start_date": "20250901"}, {"sample": false, "description": "3 BOTTLE in 1 CARTON (51672-2152-9)  / 60 mL in 1 BOTTLE", "package_ndc": "51672-2152-9", "marketing_start_date": "20250901"}], "brand_name": "Minoxidil Topical Solution 2%", "product_id": "51672-2152_4c3823f2-ce4b-afea-e063-6294a90a03c0", "dosage_form": "SOLUTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "51672-2152", "generic_name": "Minoxidil Topical Solution 2%", "labeler_name": "SUN PHARMACEUTICAL INDUSTRIES, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Minoxidil Topical Solution 2%", "active_ingredients": [{"name": "MINOXIDIL", "strength": "20 mg/mL"}], "application_number": "ANDA218175", "marketing_category": "ANDA", "marketing_start_date": "20250901", "listing_expiration_date": "20271231"}