Package 14789-107-10

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 14789-107-10
Digits Only 1478910710
Product NDC 14789-107
Description

24 BAG in 1 BOX (14789-107-10) / 100 mL in 1 BAG (14789-107-16)

Marketing

Marketing Status
Marketed Since 2021-04-02
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "fd507baf-f17a-4294-af56-ca6a5052cb1e", "openfda": {"upc": ["0314789107165", "0314789107080", "0314789109169", "0314789108162", "0314789108087"], "unii": ["660YQ98I10"], "rxcui": ["312507", "1860239", "1860241", "1860463", "1860466"], "spl_set_id": ["765ef38c-df36-46d1-9062-61e30ff46a86"], "manufacturer_name": ["Nexus Pharamaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BAG in 1 BOX (14789-107-05)  / 50 mL in 1 BAG (14789-107-08)", "package_ndc": "14789-107-05", "marketing_start_date": "20210228"}, {"sample": false, "description": "24 BAG in 1 BOX (14789-107-10)  / 100 mL in 1 BAG (14789-107-16)", "package_ndc": "14789-107-10", "marketing_start_date": "20210402"}], "brand_name": "Potassium Chloride", "product_id": "14789-107_fd507baf-f17a-4294-af56-ca6a5052cb1e", "dosage_form": "INJECTION", "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": "14789-107", "generic_name": "Potassium Chloride", "labeler_name": "Nexus Pharamaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "29.8 mg/mL"}], "application_number": "ANDA214727", "marketing_category": "ANDA", "marketing_start_date": "20210228", "listing_expiration_date": "20261231"}