minoxidil

Generic: minoxidil

Labeler: walgreens
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minoxidil
Generic Name minoxidil
Labeler walgreens
Dosage Form SOLUTION
Routes
TOPICAL
Active Ingredients

minoxidil 50 mg/mL

Manufacturer
Walgreens

Identifiers & Regulatory

Product NDC 0363-9973
Product ID 0363-9973_d0118cc5-f74a-4241-b0cb-8087db002f93
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075518
Listing Expiration 2026-12-31
Marketing Start 2022-10-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03639973
Hyphenated Format 0363-9973

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 (source: ndc)
Generic Name minoxidil (source: ndc)
Application Number ANDA075518 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/mL
source: ndc
Packaging
  • 3 BOTTLE, DROPPER in 1 CARTON (0363-9973-06) / 60 mL in 1 BOTTLE, DROPPER
source: ndc

Packages (1)

Ingredients (1)

minoxidil (50 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "d0118cc5-f74a-4241-b0cb-8087db002f93", "openfda": {"nui": ["N0000175379", "N0000175564"], "unii": ["5965120SH1"], "rxcui": ["311724"], "spl_set_id": ["a08edb99-3e45-4d3c-a0f8-c74bd291057a"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["Walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BOTTLE, DROPPER in 1 CARTON (0363-9973-06)  / 60 mL in 1 BOTTLE, DROPPER", "package_ndc": "0363-9973-06", "marketing_start_date": "20221014"}], "brand_name": "Minoxidil", "product_id": "0363-9973_d0118cc5-f74a-4241-b0cb-8087db002f93", "dosage_form": "SOLUTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "0363-9973", "generic_name": "Minoxidil", "labeler_name": "Walgreens", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Minoxidil", "active_ingredients": [{"name": "MINOXIDIL", "strength": "50 mg/mL"}], "application_number": "ANDA075518", "marketing_category": "ANDA", "marketing_start_date": "20221014", "listing_expiration_date": "20261231"}