Package 80513-100-01

Brand: docusate sodium, extra strength 250 mg

Generic: docusate sodium
NDC Package

Package Facts

Identity

Package NDC 80513-100-01
Digits Only 8051310001
Product NDC 80513-100
Product ID 80513-100_220d2464-6ee6-10d6-e063-6394a90a4f39
Description

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

Marketing

Marketing Status
Marketed Since 2022-09-15
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": "220d2464-6ee6-10d6-e063-6394a90a4f39", "openfda": {"unii": ["F05Q2T2JA0"], "rxcui": ["1245468"], "spl_set_id": ["e8be12c5-c591-eadd-e053-2a95a90a431b"], "manufacturer_name": ["Advanced Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, GELATIN COATED in 1 BOTTLE (80513-100-01)", "package_ndc": "80513-100-01", "marketing_start_date": "20220915"}], "brand_name": "DOCUSATE SODIUM, EXTRA STRENGTH 250 MG", "product_id": "80513-100_220d2464-6ee6-10d6-e063-6394a90a4f39", "dosage_form": "CAPSULE, GELATIN COATED", "product_ndc": "80513-100", "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": "20220915", "listing_expiration_date": "20261231"}