minoxidil

Generic: minoxidil

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minoxidil
Generic Name minoxidil
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

minoxidil 2.5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7758
Product ID 50090-7758_fab080f5-4064-4a72-8a22-851ce76813f8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071826
Listing Expiration 2026-12-31
Marketing Start 1988-11-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907758
Hyphenated Format 50090-7758

Supplemental Identifiers

RxCUI
197987
UNII
5965120SH1
NUI
N0000175379 N0000175564

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 ANDA071826 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (50090-7758-0)
source: ndc

Packages (1)

50090-7758-0 90 TABLET in 1 BOTTLE (50090-7758-0)

Ingredients (1)

minoxidil (2.5 mg/1)

Linked Drug Pages (1)

Minoxidil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fab080f5-4064-4a72-8a22-851ce76813f8", "openfda": {"nui": ["N0000175379", "N0000175564"], "unii": ["5965120SH1"], "rxcui": ["197987"], "spl_set_id": ["6c85c69e-b5af-4e98-aacf-f65ad15d00d7"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7758-0)", "package_ndc": "50090-7758-0", "marketing_start_date": "20251105"}], "brand_name": "Minoxidil", "product_id": "50090-7758_fab080f5-4064-4a72-8a22-851ce76813f8", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "50090-7758", "generic_name": "Minoxidil", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minoxidil", "active_ingredients": [{"name": "MINOXIDIL", "strength": "2.5 mg/1"}], "application_number": "ANDA071826", "marketing_category": "ANDA", "marketing_start_date": "19881114", "listing_expiration_date": "20261231"}