Package 59726-778-10

Brand: stool softener laxative

Generic: docusate sodium and sennosides
NDC Package

Package Facts

Identity

Package NDC 59726-778-10
Digits Only 5972677810
Product NDC 59726-778
Description

100 TABLET in 1 BOTTLE (59726-778-10)

Marketing

Marketing Status
Discontinued 2027-03-27
Brand stool softener laxative
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": "7fc75843-4bdd-4d57-a2f4-4d82171553fc", "openfda": {"upc": ["0359726885102"], "unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["84ee167d-18f2-4381-ba9e-8500869e6ef9"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59726-778-10)", "package_ndc": "59726-778-10", "marketing_end_date": "20270327", "marketing_start_date": "20210326"}], "brand_name": "Stool Softener Laxative", "product_id": "59726-778_7fc75843-4bdd-4d57-a2f4-4d82171553fc", "dosage_form": "TABLET", "product_ndc": "59726-778", "generic_name": "docusate sodium and sennosides", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stool Softener Laxative", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "50 mg/1"}, {"name": "SENNOSIDES", "strength": "8.6 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20270327", "marketing_start_date": "20210326"}