minoxidil

Generic: minoxidil

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minoxidil
Generic Name minoxidil
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

minoxidil 2.5 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-278
Product ID 72789-278_2bedbd10-32ea-e55a-e063-6394a90a65f5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072709
Listing Expiration 2026-12-31
Marketing Start 1995-12-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789278
Hyphenated Format 72789-278

Supplemental Identifiers

RxCUI
197987
UPC
0372789278018
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 ANDA072709 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (72789-278-01)
source: ndc

Packages (1)

72789-278-01 100 TABLET in 1 BOTTLE, PLASTIC (72789-278-01)

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": "2bedbd10-32ea-e55a-e063-6394a90a65f5", "openfda": {"nui": ["N0000175379", "N0000175564"], "upc": ["0372789278018"], "unii": ["5965120SH1"], "rxcui": ["197987"], "spl_set_id": ["5fea137a-bc88-4b24-85db-538c90ad1870"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-278-01)", "package_ndc": "72789-278-01", "marketing_start_date": "20221007"}], "brand_name": "MINOXIDIL", "product_id": "72789-278_2bedbd10-32ea-e55a-e063-6394a90a65f5", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "72789-278", "generic_name": "minoxidil", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MINOXIDIL", "active_ingredients": [{"name": "MINOXIDIL", "strength": "2.5 mg/1"}], "application_number": "ANDA072709", "marketing_category": "ANDA", "marketing_start_date": "19951214", "listing_expiration_date": "20261231"}