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 10 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7760
Product ID 50090-7760_9912a946-471e-4e0c-addf-373f401da0c9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071839
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 500907760
Hyphenated Format 50090-7760

Supplemental Identifiers

RxCUI
197986
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 ANDA071839 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (50090-7760-2)
source: ndc

Packages (1)

50090-7760-2 90 TABLET in 1 BOTTLE (50090-7760-2)

Ingredients (1)

minoxidil (10 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": "9912a946-471e-4e0c-addf-373f401da0c9", "openfda": {"nui": ["N0000175379", "N0000175564"], "unii": ["5965120SH1"], "rxcui": ["197986"], "spl_set_id": ["f00f3370-0313-4ce0-be7d-80db4477d9ae"], "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 (50090-7760-2)", "package_ndc": "50090-7760-2", "marketing_start_date": "20251106"}], "brand_name": "Minoxidil", "product_id": "50090-7760_9912a946-471e-4e0c-addf-373f401da0c9", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "50090-7760", "generic_name": "Minoxidil", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minoxidil", "active_ingredients": [{"name": "MINOXIDIL", "strength": "10 mg/1"}], "application_number": "ANDA071839", "marketing_category": "ANDA", "marketing_start_date": "19881114", "listing_expiration_date": "20261231"}