minoxidil

Generic: minoxidil

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minoxidil
Generic Name minoxidil
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

minoxidil 2.5 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-240
Product ID 82804-240_a0066eac-cb58-49ef-a480-105cb1043c2b
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 82804240
Hyphenated Format 82804-240

Supplemental Identifiers

RxCUI
197987
UPC
0382804240302
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
  • 30 TABLET in 1 BOTTLE (82804-240-30)
source: ndc

Packages (1)

82804-240-30 30 TABLET in 1 BOTTLE (82804-240-30)

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": "a0066eac-cb58-49ef-a480-105cb1043c2b", "openfda": {"nui": ["N0000175379", "N0000175564"], "upc": ["0382804240302"], "unii": ["5965120SH1"], "rxcui": ["197987"], "spl_set_id": ["a0066eac-cb58-49ef-a480-105cb1043c2b"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-240-30)", "package_ndc": "82804-240-30", "marketing_start_date": "20250905"}], "brand_name": "Minoxidil", "product_id": "82804-240_a0066eac-cb58-49ef-a480-105cb1043c2b", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "82804-240", "generic_name": "Minoxidil", "labeler_name": "Proficient Rx LP", "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"}