Package 21130-878-20

Brand: stool softener plus stimulant laxative

Generic: docusate sodium and sennosides
NDC Package

Package Facts

Identity

Package NDC 21130-878-20
Digits Only 2113087820
Product NDC 21130-878
Product ID 21130-878_047a9d14-a528-4ac5-8a25-ed236e4a3baa
Description

200 TABLET in 1 BOTTLE, PLASTIC (21130-878-20)

Marketing

Marketing Status
Marketed Since 2020-09-30
Brand stool softener plus stimulant laxative
Generic docusate sodium and sennosides
Sample Package No

Linked Drug Pages (1)

Stool Softener Plus Stimulant Laxative ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "047a9d14-a528-4ac5-8a25-ed236e4a3baa", "openfda": {"upc": ["0321130778899"], "unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["6bc9ea37-31b8-4a6d-9b2d-2c80bad4f30d"], "manufacturer_name": ["Safeway, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE, PLASTIC (21130-878-20)", "package_ndc": "21130-878-20", "marketing_start_date": "20200930"}], "brand_name": "Stool Softener Plus Stimulant Laxative", "product_id": "21130-878_047a9d14-a528-4ac5-8a25-ed236e4a3baa", "dosage_form": "TABLET", "product_ndc": "21130-878", "generic_name": "docusate sodium and sennosides", "labeler_name": "Safeway, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stool Softener", "brand_name_suffix": "Plus 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": "20200930", "listing_expiration_date": "20261231"}