Package 49873-404-01

Brand: sankaijo

Generic: docusate sodium, sennosides
NDC Package

Package Facts

Identity

Package NDC 49873-404-01
Digits Only 4987340401
Product NDC 49873-404
Product ID 49873-404_0b54b2d1-83e7-3a18-e063-6394a90a5b58
Description

1 BOTTLE in 1 CARTON (49873-404-01) / 150 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2002-12-20
Brand sankaijo
Generic docusate sodium, sennosides
Sample Package No

Linked Drug Pages (1)

Sankaijo ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0b54b2d1-83e7-3a18-e063-6394a90a5b58", "openfda": {"unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["1235252"], "spl_set_id": ["83c0d52b-f7e2-40b0-a01b-1ccee78f8f1b"], "manufacturer_name": ["Sato Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (49873-404-01)  / 150 TABLET in 1 BOTTLE", "package_ndc": "49873-404-01", "marketing_start_date": "20021220"}], "brand_name": "Sankaijo", "product_id": "49873-404_0b54b2d1-83e7-3a18-e063-6394a90a5b58", "dosage_form": "TABLET", "product_ndc": "49873-404", "generic_name": "docusate sodium, sennosides", "labeler_name": "Sato Pharmaceutical Co., Ltd.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sankaijo", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "8.33 mg/1"}, {"name": "SENNOSIDES", "strength": "1.36 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20021220", "listing_expiration_date": "20261231"}