Package 63868-875-01

Brand: stool softener stimulant laxative

Generic: docusate sodium and sennosides
NDC Package

Package Facts

Identity

Package NDC 63868-875-01
Digits Only 6386887501
Product NDC 63868-875
Description

100 TABLET in 1 BOTTLE, PLASTIC (63868-875-01)

Marketing

Marketing Status
Marketed Since 2018-12-31
Brand stool softener stimulant 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": "7309543d-0d54-44ee-9635-302caa83fed5", "openfda": {"upc": ["0635515997165"], "unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["9467e1f7-19bb-4fb3-853b-75c4d28bb9a9"], "manufacturer_name": ["QUALITY CHOICE (Chain Drug Marketing Association)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (63868-875-01)", "package_ndc": "63868-875-01", "marketing_start_date": "20181231"}], "brand_name": "Stool Softener Stimulant laxative", "product_id": "63868-875_7309543d-0d54-44ee-9635-302caa83fed5", "dosage_form": "TABLET", "product_ndc": "63868-875", "generic_name": "docusate sodium and sennosides", "labeler_name": "QUALITY CHOICE (Chain Drug Marketing Association)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stool Softener", "brand_name_suffix": "Stimulant 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_start_date": "20181231", "listing_expiration_date": "20261231"}