0591-5347
Generic: probenecid
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
Generic Name
probenecid
Labeler
actavis pharma, inc.
Dosage Form
TABLET, FILM COATED
Active Ingredients
probenecid 500 mg/1
Identifiers & Regulatory
Product NDC
0591-5347
Product ID
0591-5347_94eda56c-ea2b-47df-883f-1d51dcd5f964
Product Type
DRUG FOR FURTHER PROCESSING
Marketing Category
DRUG FOR FURTHER PROCESSING
Listing Expiration
2026-12-31
Marketing Start
1983-07-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05915347
Hyphenated Format
0591-5347
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
probenecid (source: label)
Generic Name
probenecid (source: ndc)
Application Number
ANDA084442 (source: label)
Routes
source: label
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 14000 TABLET, FILM COATED in 1 BAG (0591-5347-00)
- 16812 TABLET, FILM COATED in 1 CONTAINER (0591-5347-77)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "94eda56c-ea2b-47df-883f-1d51dcd5f964", "openfda": {}, "finished": false, "packaging": [{"description": "14000 TABLET, FILM COATED in 1 BAG (0591-5347-00)", "package_ndc": "0591-5347-00", "marketing_start_date": "01-JUL-83"}, {"description": "16812 TABLET, FILM COATED in 1 CONTAINER (0591-5347-77)", "package_ndc": "0591-5347-77", "marketing_start_date": "22-JUL-24"}], "product_id": "0591-5347_94eda56c-ea2b-47df-883f-1d51dcd5f964", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0591-5347", "generic_name": "Probenecid", "labeler_name": "Actavis Pharma, Inc.", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "PROBENECID", "strength": "500 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_start_date": "19830701", "listing_expiration_date": "20261231"}