minoxidil

Generic: minoxidil

Labeler: p & l development, llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minoxidil
Generic Name minoxidil
Labeler p & l development, llc
Dosage Form AEROSOL, FOAM
Routes
TOPICAL
Active Ingredients

minoxidil 50 mg/mL

Manufacturer
P & L Development, LLC

Identifiers & Regulatory

Product NDC 59726-125
Product ID 59726-125_daa285c7-be37-4292-9966-13bd7ee54bc2
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA208092
Listing Expiration 2027-12-31
Marketing Start 2023-10-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59726125
Hyphenated Format 59726-125

Supplemental Identifiers

RxCUI
645146
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 ANDA208092 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/mL
source: ndc
Packaging
  • 1 CAN in 1 PACKAGE (59726-125-60) / 60 mL in 1 CAN
  • 3 CAN in 1 PACKAGE (59726-125-70) / 60 mL in 1 CAN
source: ndc

Packages (2)

59726-125-60 1 CAN in 1 PACKAGE (59726-125-60) / 60 mL in 1 CAN 59726-125-70 3 CAN in 1 PACKAGE (59726-125-70) / 60 mL in 1 CAN

Ingredients (1)

minoxidil (50 mg/mL)

Linked Drug Pages (1)

Minoxidil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "daa285c7-be37-4292-9966-13bd7ee54bc2", "openfda": {"nui": ["N0000175379", "N0000175564"], "unii": ["5965120SH1"], "rxcui": ["645146"], "spl_set_id": ["869ce741-3094-4123-9059-0669f3591b2f"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 CAN in 1 PACKAGE (59726-125-60)  / 60 mL in 1 CAN", "package_ndc": "59726-125-60", "marketing_start_date": "20231001"}, {"sample": false, "description": "3 CAN in 1 PACKAGE (59726-125-70)  / 60 mL in 1 CAN", "package_ndc": "59726-125-70", "marketing_start_date": "20231001"}], "brand_name": "Minoxidil", "product_id": "59726-125_daa285c7-be37-4292-9966-13bd7ee54bc2", "dosage_form": "AEROSOL, FOAM", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "59726-125", "generic_name": "Minoxidil", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Minoxidil", "active_ingredients": [{"name": "MINOXIDIL", "strength": "50 mg/mL"}], "application_number": "ANDA208092", "marketing_category": "ANDA", "marketing_start_date": "20231001", "listing_expiration_date": "20271231"}