Package 81033-022-50
Brand: docusate sodium oral liquid
Generic: docusate sodium oral liquidPackage Facts
Identity
Package NDC
81033-022-50
Digits Only
8103302250
Product NDC
81033-022
Description
100 CUP, UNIT-DOSE in 1 CASE (81033-022-50) / 10 mL in 1 CUP, UNIT-DOSE (81033-022-10)
Marketing
Marketing Status
Brand
docusate sodium oral liquid
Generic
docusate sodium oral liquid
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "331277b8-8305-d082-e063-6394a90a4dd3", "openfda": {"unii": ["F05Q2T2JA0"], "rxcui": ["1248119"], "spl_set_id": ["331277b8-8304-d082-e063-6394a90a4dd3"], "manufacturer_name": ["Kesin Pharma Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (81033-022-50) / 10 mL in 1 CUP, UNIT-DOSE (81033-022-10)", "package_ndc": "81033-022-50", "marketing_start_date": "20250401"}], "brand_name": "Docusate Sodium Oral Liquid", "product_id": "81033-022_331277b8-8305-d082-e063-6394a90a4dd3", "dosage_form": "LIQUID", "product_ndc": "81033-022", "generic_name": "Docusate Sodium Oral Liquid", "labeler_name": "Kesin Pharma Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Docusate Sodium Oral Liquid", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "100 mg/10mL"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250401", "listing_expiration_date": "20261231"}