minoxidil

Generic: minoxidil

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

minoxidil 2.5 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3794
Product ID 68071-3794_48862260-1894-0602-e063-6294a90a1eff
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071826
Listing Expiration 2027-12-31
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 680713794
Hyphenated Format 68071-3794

Supplemental Identifiers

RxCUI
197987
UPC
0368071379433
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 (68071-3794-3)
source: ndc

Packages (1)

68071-3794-3 30 TABLET in 1 BOTTLE (68071-3794-3)

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": "48862260-1894-0602-e063-6294a90a1eff", "openfda": {"nui": ["N0000175379", "N0000175564"], "upc": ["0368071379433"], "unii": ["5965120SH1"], "rxcui": ["197987"], "spl_set_id": ["2e5a2976-06fb-43f9-e063-6294a90a3bf5"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3794-3)", "package_ndc": "68071-3794-3", "marketing_start_date": "20250217"}], "brand_name": "Minoxidil", "product_id": "68071-3794_48862260-1894-0602-e063-6294a90a1eff", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "68071-3794", "generic_name": "Minoxidil", "labeler_name": "NuCare Pharmaceuticals, Inc.", "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": "20271231"}