Package 72162-2237-1

Brand: probenecid

Generic: probenecid
NDC Package

Package Facts

Identity

Package NDC 72162-2237-1
Digits Only 7216222371
Product NDC 72162-2237
Product ID 72162-2237_8c261b93-98b4-46ce-a713-11d3b2d7cd13
Description

100 TABLET, FILM COATED in 1 BOTTLE (72162-2237-1)

Marketing

Marketing Status
Marketed Since 2024-01-26
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": "8c261b93-98b4-46ce-a713-11d3b2d7cd13", "openfda": {"unii": ["PO572Z7917"], "rxcui": ["198152"], "spl_set_id": ["6aec72b5-a9f4-45a3-82a6-7d3de64ba5e5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-2237-1)", "package_ndc": "72162-2237-1", "marketing_start_date": "20240126"}], "brand_name": "Probenecid", "product_id": "72162-2237_8c261b93-98b4-46ce-a713-11d3b2d7cd13", "dosage_form": "TABLET, FILM COATED", "product_ndc": "72162-2237", "generic_name": "Probenecid", "labeler_name": "Bryant Ranch Prepack", "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"}