Package 16571-831-01

Brand: probenecid

Generic: probenecid
NDC Package

Package Facts

Identity

Package NDC 16571-831-01
Digits Only 1657183101
Product NDC 16571-831
Product ID 16571-831_5b9e2e37-77b7-464f-9bc8-ff678643d773
Description

100 TABLET in 1 CONTAINER (16571-831-01)

Marketing

Marketing Status
Marketed Since 2023-11-20
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": "5b9e2e37-77b7-464f-9bc8-ff678643d773", "openfda": {"unii": ["PO572Z7917"], "rxcui": ["198152"], "spl_set_id": ["f2375d90-4132-4fb6-aee7-c4f9d11e98d5"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 CONTAINER (16571-831-01)", "package_ndc": "16571-831-01", "marketing_start_date": "20231120"}, {"sample": false, "description": "1000 TABLET in 1 CONTAINER (16571-831-10)", "package_ndc": "16571-831-10", "marketing_start_date": "20231120"}], "brand_name": "Probenecid", "product_id": "16571-831_5b9e2e37-77b7-464f-9bc8-ff678643d773", "dosage_form": "TABLET", "product_ndc": "16571-831", "generic_name": "Probenecid", "labeler_name": "Rising Pharma Holdings, Inc.", "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": "20271231"}