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 71205-757
Product ID 71205-757_637718aa-a453-4acd-a992-590d637b63a3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071344
Listing Expiration 2026-12-31
Marketing Start 2009-10-26

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205757
Hyphenated Format 71205-757

Supplemental Identifiers

RxCUI
197987
UPC
0371205757304
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 ANDA071344 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (71205-757-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (71205-757-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (71205-757-90)
source: ndc

Packages (3)

71205-757-30 30 TABLET in 1 BOTTLE, PLASTIC (71205-757-30) 71205-757-60 60 TABLET in 1 BOTTLE, PLASTIC (71205-757-60) 71205-757-90 90 TABLET in 1 BOTTLE, PLASTIC (71205-757-90)

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": "637718aa-a453-4acd-a992-590d637b63a3", "openfda": {"nui": ["N0000175379", "N0000175564"], "upc": ["0371205757304"], "unii": ["5965120SH1"], "rxcui": ["197987"], "spl_set_id": ["637718aa-a453-4acd-a992-590d637b63a3"], "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, PLASTIC (71205-757-30)", "package_ndc": "71205-757-30", "marketing_start_date": "20230207"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (71205-757-60)", "package_ndc": "71205-757-60", "marketing_start_date": "20230207"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (71205-757-90)", "package_ndc": "71205-757-90", "marketing_start_date": "20230207"}], "brand_name": "Minoxidil", "product_id": "71205-757_637718aa-a453-4acd-a992-590d637b63a3", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "71205-757", "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": "ANDA071344", "marketing_category": "ANDA", "marketing_start_date": "20091026", "listing_expiration_date": "20261231"}