0591-5543
Generic: allopurinol
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
Generic Name
allopurinol
Labeler
actavis pharma, inc.
Dosage Form
TABLET
Active Ingredients
allopurinol 100 mg/1
Identifiers & Regulatory
Product NDC
0591-5543
Product ID
0591-5543_531594e1-34a6-49c3-a3ad-7e697af83807
Product Type
DRUG FOR FURTHER PROCESSING
Marketing Category
DRUG FOR FURTHER PROCESSING
Listing Expiration
2026-12-31
Marketing Start
2009-04-06
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05915543
Hyphenated Format
0591-5543
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
allopurinol (source: label)
Generic Name
allopurinol (source: ndc)
Application Number
NDA018832 (source: label)
Routes
source: label
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 31700 TABLET in 1 BAG (0591-5543-00)
- 38088 TABLET in 1 CONTAINER (0591-5543-77)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "531594e1-34a6-49c3-a3ad-7e697af83807", "openfda": {}, "finished": false, "packaging": [{"description": "31700 TABLET in 1 BAG (0591-5543-00)", "package_ndc": "0591-5543-00", "marketing_start_date": "06-APR-09"}, {"description": "38088 TABLET in 1 CONTAINER (0591-5543-77)", "package_ndc": "0591-5543-77", "marketing_start_date": "11-JUN-24"}], "product_id": "0591-5543_531594e1-34a6-49c3-a3ad-7e697af83807", "dosage_form": "TABLET", "product_ndc": "0591-5543", "generic_name": "Allopurinol", "labeler_name": "Actavis Pharma, Inc.", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_start_date": "20090406", "listing_expiration_date": "20261231"}