Package 59726-755-10

Brand: stool softener laxative

Generic: docusate sodium and sennosides
NDC Package

Package Facts

Identity

Package NDC 59726-755-10
Digits Only 5972675510
Product NDC 59726-755
Description

100 TABLET in 1 BOTTLE, PLASTIC (59726-755-10)

Marketing

Marketing Status
Discontinued 2026-12-31
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": "22665a75-5a36-412b-a6b4-dd2c04f2755e", "openfda": {"upc": ["0359726885102"], "unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["a168b018-207b-451b-8e66-ad8c5c0e7900"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (59726-755-10)", "package_ndc": "59726-755-10", "marketing_end_date": "20261231", "marketing_start_date": "20210326"}], "brand_name": "Stool Softener Laxative", "product_id": "59726-755_22665a75-5a36-412b-a6b4-dd2c04f2755e", "dosage_form": "TABLET", "product_ndc": "59726-755", "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": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261231", "marketing_start_date": "20210326"}