Package 0527-1367-10

Brand: probenecid

Generic: probenecid
NDC Package

Package Facts

Identity

Package NDC 0527-1367-10
Digits Only 0527136710
Product NDC 0527-1367
Product ID 0527-1367_8679dae4-b649-458d-962b-2afb0f491d2a
Description

1000 TABLET, FILM COATED in 1 BOTTLE (0527-1367-10)

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": "8679dae4-b649-458d-962b-2afb0f491d2a", "openfda": {"upc": ["0305271367013"], "unii": ["PO572Z7917"], "rxcui": ["198152"], "spl_set_id": ["ab497fd8-00c3-4364-b003-b39d21fbdf38"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0527-1367-01)", "package_ndc": "0527-1367-01", "marketing_start_date": "19760729"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (0527-1367-10)", "package_ndc": "0527-1367-10", "marketing_start_date": "19760729"}], "brand_name": "Probenecid", "product_id": "0527-1367_8679dae4-b649-458d-962b-2afb0f491d2a", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0527-1367", "generic_name": "Probenecid", "labeler_name": "Lannett Company, 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"}