Package 72162-2386-1

Brand: probenecid

Generic: probenecid
NDC Package

Package Facts

Identity

Package NDC 72162-2386-1
Digits Only 7216223861
Product NDC 72162-2386
Product ID 72162-2386_c2638148-9137-410b-b35b-671a77b52412
Description

100 TABLET in 1 CONTAINER (72162-2386-1)

Marketing

Marketing Status
Marketed Since 2024-08-15
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": "c2638148-9137-410b-b35b-671a77b52412", "openfda": {"unii": ["PO572Z7917"], "rxcui": ["198152"], "spl_set_id": ["a4f4b3e1-44a9-4b3a-9f7f-f9749ed451ca"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 CONTAINER (72162-2386-1)", "package_ndc": "72162-2386-1", "marketing_start_date": "20240815"}], "brand_name": "Probenecid", "product_id": "72162-2386_c2638148-9137-410b-b35b-671a77b52412", "dosage_form": "TABLET", "product_ndc": "72162-2386", "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": "ANDA217020", "marketing_category": "ANDA", "marketing_start_date": "20231120", "listing_expiration_date": "20261231"}