Package 0591-5347-10

Brand: probenecid

Generic: probenecid
NDC Package

Package Facts

Identity

Package NDC 0591-5347-10
Digits Only 0591534710
Product NDC 0591-5347
Description

1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-5347-10)

Marketing

Marketing Status
Marketed Since 1983-07-01
Brand probenecid
Generic probenecid
Sample Package No

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"}