Package 0404-9936-20

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 0404-9936-20
Digits Only 0404993620
Product NDC 0404-9936
Product ID 0404-9936_86d210da-05db-45c6-b2fd-4d6aa79484fa
Description

1 VIAL, SINGLE-DOSE in 1 BAG (0404-9936-20) / 20 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2022-01-13
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "86d210da-05db-45c6-b2fd-4d6aa79484fa", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1860132", "1860139"], "spl_set_id": ["bf8e8ac7-e6a8-4571-a0ea-7bcab89290f6"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9936-10)  / 5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9936-10", "marketing_start_date": "20220113"}, {"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9936-20)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9936-20", "marketing_start_date": "20220113"}], "brand_name": "Potassium Chloride", "product_id": "0404-9936_86d210da-05db-45c6-b2fd-4d6aa79484fa", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0404-9936", "generic_name": "Potassium Chloride", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "2 meq/mL"}], "application_number": "ANDA088901", "marketing_category": "ANDA", "marketing_start_date": "20220113", "listing_expiration_date": "20261231"}