0591-2405
Generic: ambrisentan
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
Generic Name
ambrisentan
Labeler
actavis pharma, inc.
Dosage Form
TABLET, FILM COATED
Active Ingredients
ambrisentan 5 mg/1
Identifiers & Regulatory
Product NDC
0591-2405
Product ID
0591-2405_acd86326-b7d1-4a7c-90ec-1c13411b0a56
Product Type
DRUG FOR FURTHER PROCESSING
Marketing Category
DRUG FOR FURTHER PROCESSING
Listing Expiration
2026-12-31
Marketing Start
2019-03-28
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05912405
Hyphenated Format
0591-2405
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
ambrisentan (source: label)
Generic Name
ambrisentan (source: ndc)
Application Number
ANDA208252 (source: label)
Routes
source: label
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 88261 TABLET, FILM COATED in 1 BOX (0591-2405-00)
- 105912 TABLET, FILM COATED in 1 CONTAINER (0591-2405-77)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "acd86326-b7d1-4a7c-90ec-1c13411b0a56", "openfda": {}, "finished": false, "packaging": [{"description": "88261 TABLET, FILM COATED in 1 BOX (0591-2405-00)", "package_ndc": "0591-2405-00", "marketing_start_date": "28-MAR-19"}, {"description": "105912 TABLET, FILM COATED in 1 CONTAINER (0591-2405-77)", "package_ndc": "0591-2405-77", "marketing_start_date": "07-AUG-24"}], "product_id": "0591-2405_acd86326-b7d1-4a7c-90ec-1c13411b0a56", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0591-2405", "generic_name": "Ambrisentan", "labeler_name": "Actavis Pharma, Inc.", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "AMBRISENTAN", "strength": "5 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_start_date": "20190328", "listing_expiration_date": "20261231"}