Package 21130-829-20

Brand: stool softener plus stimulant laxative

Generic: docusate sodium and sennosides
NDC Package

Package Facts

Identity

Package NDC 21130-829-20
Digits Only 2113082920
Product NDC 21130-829
Product ID 21130-829_b2e04adb-fa28-426c-8bb9-d4882fb21c6d
Description

200 TABLET in 1 BOTTLE, PLASTIC (21130-829-20)

Marketing

Marketing Status
Marketed Since 2018-12-31
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": "b2e04adb-fa28-426c-8bb9-d4882fb21c6d", "openfda": {"upc": ["0052000002157"], "unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["c0898583-4bbb-41d5-9e84-00cca823024f"], "manufacturer_name": ["Safeway, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE, PLASTIC (21130-829-20)", "package_ndc": "21130-829-20", "marketing_start_date": "20181231"}], "brand_name": "Stool Softener Plus Stimulant Laxative", "product_id": "21130-829_b2e04adb-fa28-426c-8bb9-d4882fb21c6d", "dosage_form": "TABLET", "product_ndc": "21130-829", "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": "20181231", "listing_expiration_date": "20261231"}