0591-5642
Generic: minoxidil
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
Generic Name
minoxidil
Labeler
actavis pharma, inc.
Dosage Form
TABLET
Active Ingredients
minoxidil 2.5 mg/1
Identifiers & Regulatory
Product NDC
0591-5642
Product ID
0591-5642_dc3a1d2b-295f-41aa-94c8-af88a308ca7a
Product Type
DRUG FOR FURTHER PROCESSING
Marketing Category
DRUG FOR FURTHER PROCESSING
Listing Expiration
2026-12-31
Marketing Start
2009-10-26
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05915642
Hyphenated Format
0591-5642
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: label)
Generic Name
minoxidil (source: ndc)
Application Number
ANDA071344 (source: label)
Routes
source: label
Resolved Composition
Strengths
- 2.5 mg/1
Packaging
- 91000 TABLET in 1 BAG (0591-5642-00)
- 109092 TABLET in 1 CONTAINER (0591-5642-77)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "dc3a1d2b-295f-41aa-94c8-af88a308ca7a", "openfda": {}, "finished": false, "packaging": [{"description": "91000 TABLET in 1 BAG (0591-5642-00)", "package_ndc": "0591-5642-00", "marketing_start_date": "26-OCT-09"}, {"description": "109092 TABLET in 1 CONTAINER (0591-5642-77)", "package_ndc": "0591-5642-77", "marketing_start_date": "11-JUN-24"}], "product_id": "0591-5642_dc3a1d2b-295f-41aa-94c8-af88a308ca7a", "dosage_form": "TABLET", "product_ndc": "0591-5642", "generic_name": "Minoxidil", "labeler_name": "Actavis Pharma, Inc.", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "MINOXIDIL", "strength": "2.5 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_start_date": "20091026", "listing_expiration_date": "20261231"}