Package 50804-304-10

Brand: stimulant laxative plus stool softener

Generic: docusate sodium and sennosides
NDC Package

Package Facts

Identity

Package NDC 50804-304-10
Digits Only 5080430410
Product NDC 50804-304
Description

100 TABLET, FILM COATED in 1 BOTTLE (50804-304-10)

Marketing

Marketing Status
Marketed Since 2024-06-01
Brand stimulant laxative plus stool softener
Generic docusate sodium and sennosides
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1dd8d066-303d-d5c1-e063-6394a90a5b71", "openfda": {"upc": ["0846036009750"], "unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["17cdef7b-71bf-b4a6-e063-6294a90a5b74"], "manufacturer_name": ["GOOD SENSE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50804-304-10)", "package_ndc": "50804-304-10", "marketing_start_date": "20240601"}], "brand_name": "Stimulant Laxative Plus Stool Softener", "product_id": "50804-304_1dd8d066-303d-d5c1-e063-6394a90a5b71", "dosage_form": "TABLET, FILM COATED", "product_ndc": "50804-304", "generic_name": "Docusate Sodium and Sennosides", "labeler_name": "GOOD SENSE", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stimulant Laxative Plus Stool Softener", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "50 mg/1"}, {"name": "SENNOSIDES", "strength": "8.6 mg/1"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240601", "listing_expiration_date": "20261231"}