Package 0121-0935-40

Brand: docusate sodium

Generic: docusate sodium
NDC Package

Package Facts

Identity

Package NDC 0121-0935-40
Digits Only 0121093540
Product NDC 0121-0935
Product ID 0121-0935_5cfc4685-c885-4303-a988-5009cbd8e57b
Description

4 TRAY in 1 CASE (0121-0935-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-0935-05)

Marketing

Marketing Status
Marketed Since 2021-08-16
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": "5cfc4685-c885-4303-a988-5009cbd8e57b", "openfda": {"unii": ["F05Q2T2JA0"], "rxcui": ["1245686"], "spl_set_id": ["e975a3f1-0e1f-4fb8-9c5f-baa75e12f2a5"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 TRAY in 1 CASE (0121-0935-40)  / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-0935-05)", "package_ndc": "0121-0935-40", "marketing_start_date": "20210816"}], "brand_name": "Docusate Sodium", "product_id": "0121-0935_5cfc4685-c885-4303-a988-5009cbd8e57b", "dosage_form": "LIQUID", "product_ndc": "0121-0935", "generic_name": "Docusate Sodium", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Docusate Sodium", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "50 mg/5mL"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210816", "listing_expiration_date": "20261231"}