Package 80513-101-01

Brand: docusate sodium, extra strength 250 mg

Generic: docusate sodium
NDC Package

Package Facts

Identity

Package NDC 80513-101-01
Digits Only 8051310101
Product NDC 80513-101
Product ID 80513-101_220d3b4f-44ba-0335-e063-6294a90ad1cd
Description

100 CAPSULE, GELATIN COATED in 1 BOTTLE (80513-101-01)

Marketing

Marketing Status
Marketed Since 2023-05-25
Brand docusate sodium, extra strength 250 mg
Generic docusate sodium
Sample Package No

Linked Drug Pages (1)

DOCUSATE SODIUM, EXTRA STRENGTH 250 MG ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "220d3b4f-44ba-0335-e063-6294a90ad1cd", "openfda": {"unii": ["F05Q2T2JA0"], "rxcui": ["1245468"], "spl_set_id": ["fc8cf24e-8ca1-b3fb-e053-6294a90a7a50"], "manufacturer_name": ["Advanced Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, GELATIN COATED in 1 BOTTLE (80513-101-01)", "package_ndc": "80513-101-01", "marketing_start_date": "20230525"}], "brand_name": "DOCUSATE SODIUM, EXTRA STRENGTH 250 MG", "product_id": "80513-101_220d3b4f-44ba-0335-e063-6294a90ad1cd", "dosage_form": "CAPSULE, GELATIN COATED", "product_ndc": "80513-101", "generic_name": "DOCUSATE SODIUM", "labeler_name": "Advanced Rx LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DOCUSATE SODIUM, EXTRA STRENGTH", "brand_name_suffix": "250 MG", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "250 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230525", "listing_expiration_date": "20261231"}