minoxidil

Generic: minoxidil

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minoxidil
Generic Name minoxidil
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

minoxidil 10 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 68084-205
Product ID 68084-205_43e0ff0a-c0e4-97fc-e063-6294a90ae3dd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071839
Listing Expiration 2026-12-31
Marketing Start 2007-09-05

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68084205
Hyphenated Format 68084-205

Supplemental Identifiers

RxCUI
197986 197987
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 ANDA071839 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-205-01) / 1 TABLET in 1 BLISTER PACK (68084-205-11)
source: ndc

Packages (1)

68084-205-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-205-01) / 1 TABLET in 1 BLISTER PACK (68084-205-11)

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": "43e0ff0a-c0e4-97fc-e063-6294a90ae3dd", "openfda": {"nui": ["N0000175379", "N0000175564"], "unii": ["5965120SH1"], "rxcui": ["197986", "197987"], "spl_set_id": ["0b4fc036-9497-442b-b629-c4b386932789"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-205-01)  / 1 TABLET in 1 BLISTER PACK (68084-205-11)", "package_ndc": "68084-205-01", "marketing_start_date": "20070905"}], "brand_name": "Minoxidil", "product_id": "68084-205_43e0ff0a-c0e4-97fc-e063-6294a90ae3dd", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "68084-205", "generic_name": "Minoxidil", "labeler_name": "American Health Packaging", "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": "20070905", "listing_expiration_date": "20261231"}