Package 10135-541-01

Brand: probenecid

Generic: probenecid
NDC Package

Package Facts

Identity

Package NDC 10135-541-01
Digits Only 1013554101
Product NDC 10135-541
Product ID 10135-541_43e0b999-0f40-3c9d-e063-6294a90ae477
Description

100 TABLET, FILM COATED in 1 BOTTLE (10135-541-01)

Marketing

Marketing Status
Marketed Since 1976-07-29
Brand probenecid
Generic probenecid
Sample Package No

Linked Drug Pages (1)

Probenecid ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43e0b999-0f40-3c9d-e063-6294a90ae477", "openfda": {"unii": ["PO572Z7917"], "rxcui": ["198152"], "spl_set_id": ["5d552de5-2d18-4464-bcaf-0311fa3f080d"], "manufacturer_name": ["Marlex Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (10135-541-01)", "package_ndc": "10135-541-01", "marketing_start_date": "19760729"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (10135-541-10)", "package_ndc": "10135-541-10", "marketing_start_date": "19760729"}], "brand_name": "Probenecid", "product_id": "10135-541_43e0b999-0f40-3c9d-e063-6294a90ae477", "dosage_form": "TABLET, FILM COATED", "product_ndc": "10135-541", "generic_name": "Probenecid", "labeler_name": "Marlex Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Probenecid", "active_ingredients": [{"name": "PROBENECID", "strength": "500 mg/1"}], "application_number": "ANDA080966", "marketing_category": "ANDA", "marketing_start_date": "19760729", "listing_expiration_date": "20261231"}