Package 50488-0901-1

Brand: laxacin

Generic: docusate sodium and sennosides
NDC Package

Package Facts

Identity

Package NDC 50488-0901-1
Digits Only 5048809011
Product NDC 50488-0901
Product ID 50488-0901_1b45f6d1-4436-4b3a-813b-7043c0d0fad6
Description

100 TABLET in 1 BOTTLE (50488-0901-1)

Marketing

Marketing Status
Marketed Since 2018-10-15
Brand laxacin
Generic docusate sodium and sennosides
Sample Package No

Linked Drug Pages (1)

Laxacin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1b45f6d1-4436-4b3a-813b-7043c0d0fad6", "openfda": {"unii": ["F05Q2T2JA0", "1B5FPI42EN"], "rxcui": ["998740", "2106884"], "spl_set_id": ["0df9abaf-3997-4dde-8003-ae3d8d07cf39"], "manufacturer_name": ["Alexso, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50488-0901-1)", "package_ndc": "50488-0901-1", "marketing_start_date": "20181015"}], "brand_name": "Laxacin", "product_id": "50488-0901_1b45f6d1-4436-4b3a-813b-7043c0d0fad6", "dosage_form": "TABLET", "product_ndc": "50488-0901", "generic_name": "Docusate sodium and sennosides", "labeler_name": "Alexso, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Laxacin", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "50 mg/1"}, {"name": "SENNOSIDES A AND B", "strength": "8.6 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20181015", "listing_expiration_date": "20261231"}