probenecid

Generic: probenecid

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name probenecid
Generic Name probenecid
Labeler actavis pharma, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

probenecid 500 mg/1

Manufacturer
Actavis Pharma, Inc.

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
198152
UNII
PO572Z7917

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-5347-01)
  • 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-5347-10)
source: ndc

Packages (2)

Ingredients (1)

probenecid (500 mg/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"}