0591-2712
Generic: albendazole
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
Generic Name
albendazole
Labeler
actavis pharma, inc.
Dosage Form
TABLET, FILM COATED
Active Ingredients
albendazole 200 mg/1
Identifiers & Regulatory
Product NDC
0591-2712
Product ID
0591-2712_912be34f-be92-4e20-882a-01a2953ec9a5
Product Type
DRUG FOR FURTHER PROCESSING
Marketing Category
DRUG FOR FURTHER PROCESSING
Listing Expiration
2026-12-31
Marketing Start
2019-06-13
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05912712
Hyphenated Format
0591-2712
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
albendazole (source: label)
Generic Name
albendazole (source: ndc)
Application Number
ANDA208094 (source: label)
Routes
source: label
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 15016 TABLET, FILM COATED in 1 BOX (0591-2712-00)
- 18024 TABLET, FILM COATED in 1 CONTAINER (0591-2712-77)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "912be34f-be92-4e20-882a-01a2953ec9a5", "openfda": {}, "finished": false, "packaging": [{"description": "15016 TABLET, FILM COATED in 1 BOX (0591-2712-00)", "package_ndc": "0591-2712-00", "marketing_start_date": "13-JUN-19"}, {"description": "18024 TABLET, FILM COATED in 1 CONTAINER (0591-2712-77)", "package_ndc": "0591-2712-77", "marketing_start_date": "22-AUG-24"}], "product_id": "0591-2712_912be34f-be92-4e20-882a-01a2953ec9a5", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0591-2712", "generic_name": "Albendazole", "labeler_name": "Actavis Pharma, Inc.", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "ALBENDAZOLE", "strength": "200 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_start_date": "20190613", "listing_expiration_date": "20261231"}