probenecid
Generic: probenecid
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
probenecid
Generic Name
probenecid
Labeler
actavis pharma, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
probenecid 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0591-5347
Product ID
0591-5347_8319745d-3201-48c6-b1eb-9ff32e930872
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA084442
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
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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: ndc)
Generic Name
probenecid (source: ndc)
Application Number
ANDA084442 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-5347-01)
- 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-5347-10)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8319745d-3201-48c6-b1eb-9ff32e930872", "openfda": {"unii": ["PO572Z7917"], "rxcui": ["198152"], "spl_set_id": ["ae126418-5474-4fbe-b83c-bde8b2b4ae6e"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-5347-01)", "package_ndc": "0591-5347-01", "marketing_start_date": "19830701"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-5347-10)", "package_ndc": "0591-5347-10", "marketing_start_date": "19830701"}], "brand_name": "Probenecid", "product_id": "0591-5347_8319745d-3201-48c6-b1eb-9ff32e930872", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0591-5347", "generic_name": "Probenecid", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Probenecid", "active_ingredients": [{"name": "PROBENECID", "strength": "500 mg/1"}], "application_number": "ANDA084442", "marketing_category": "ANDA", "marketing_start_date": "19830701", "listing_expiration_date": "20261231"}