Package 48433-220-10

Brand: docusate sodium

Generic: docusate sodium
NDC Package

Package Facts

Identity

Package NDC 48433-220-10
Digits Only 4843322010
Product NDC 48433-220
Product ID 48433-220_3b918dfb-629d-4eef-ba71-d2ee2f97747f
Description

10 mL in 1 CUP, UNIT-DOSE (48433-220-10)

Marketing

Marketing Status
Marketed Since 2021-09-01
Brand docusate sodium
Generic docusate sodium
Sample Package No

Linked Drug Pages (1)

DOCUSATE SODIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3b918dfb-629d-4eef-ba71-d2ee2f97747f", "openfda": {"upc": ["0348433220405"], "unii": ["F05Q2T2JA0"], "rxcui": ["1248119"], "spl_set_id": ["efe4bf81-fb99-4755-aa23-4f8df5973be8"], "manufacturer_name": ["Safecor Health, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 CUP, UNIT-DOSE (48433-220-10)", "package_ndc": "48433-220-10", "marketing_start_date": "20210901"}], "brand_name": "DOCUSATE SODIUM", "product_id": "48433-220_3b918dfb-629d-4eef-ba71-d2ee2f97747f", "dosage_form": "LIQUID", "product_ndc": "48433-220", "generic_name": "DOCUSATE SODIUM", "labeler_name": "Safecor Health, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DOCUSATE SODIUM", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "50 mg/5mL"}], "application_number": "M334", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210901", "listing_expiration_date": "20261231"}