minoxidil

Generic: minoxidil

Labeler: avkare
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minoxidil
Generic Name minoxidil
Labeler avkare
Dosage Form TABLET
Routes
ORAL
Active Ingredients

minoxidil 2.5 mg/1

Manufacturer
AvKARE

Identifiers & Regulatory

Product NDC 42291-618
Product ID 42291-618_48e97f58-ac9b-0967-e063-6294a90a26a5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072708
Listing Expiration 2027-12-31
Marketing Start 2013-08-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42291618
Hyphenated Format 42291-618

Supplemental Identifiers

RxCUI
197986 197987
UPC
0342291618015 0342291619012
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 ANDA072708 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (42291-618-01)
source: ndc

Packages (1)

42291-618-01 100 TABLET in 1 BOTTLE (42291-618-01)

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": "48e97f58-ac9b-0967-e063-6294a90a26a5", "openfda": {"nui": ["N0000175379", "N0000175564"], "upc": ["0342291618015", "0342291619012"], "unii": ["5965120SH1"], "rxcui": ["197986", "197987"], "spl_set_id": ["02d7399f-94cc-f718-f214-587301edd138"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42291-618-01)", "package_ndc": "42291-618-01", "marketing_start_date": "20130801"}], "brand_name": "MINOXIDIL", "product_id": "42291-618_48e97f58-ac9b-0967-e063-6294a90a26a5", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "42291-618", "generic_name": "minoxidil", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MINOXIDIL", "active_ingredients": [{"name": "MINOXIDIL", "strength": "2.5 mg/1"}], "application_number": "ANDA072708", "marketing_category": "ANDA", "marketing_start_date": "20130801", "listing_expiration_date": "20271231"}