minoxidil

Generic: minoxidil

Labeler: endo usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minoxidil
Generic Name minoxidil
Labeler endo usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

minoxidil 10 mg/1

Manufacturer
Endo USA, Inc.

Identifiers & Regulatory

Product NDC 49884-257
Product ID 49884-257_d387cf20-4627-4429-8408-f240ace9df72
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 49884257
Hyphenated Format 49884-257

Supplemental Identifiers

RxCUI
197986 197987
UPC
0349884256012 0349884257057
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 ANDA071839 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (49884-257-01)
  • 500 TABLET in 1 BOTTLE (49884-257-05)
source: ndc

Packages (2)

49884-257-01 100 TABLET in 1 BOTTLE (49884-257-01) 49884-257-05 500 TABLET in 1 BOTTLE (49884-257-05)

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": "d387cf20-4627-4429-8408-f240ace9df72", "openfda": {"nui": ["N0000175379", "N0000175564"], "upc": ["0349884256012", "0349884257057"], "unii": ["5965120SH1"], "rxcui": ["197986", "197987"], "spl_set_id": ["8f3800f0-b6da-4dfe-8c32-39bb5eb0262a"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (49884-257-01)", "package_ndc": "49884-257-01", "marketing_start_date": "19881114"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (49884-257-05)", "package_ndc": "49884-257-05", "marketing_start_date": "19881114"}], "brand_name": "Minoxidil", "product_id": "49884-257_d387cf20-4627-4429-8408-f240ace9df72", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "49884-257", "generic_name": "Minoxidil", "labeler_name": "Endo USA, Inc.", "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"}