Package 14789-137-05

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 14789-137-05
Digits Only 1478913705
Product NDC 14789-137
Product ID 14789-137_0ce97a26-ec41-4c7a-8198-4850a9dc81f7
Description

25 VIAL, GLASS in 1 CARTON (14789-137-05) / 20 mL in 1 VIAL, GLASS (14789-137-07)

Marketing

Marketing Status
Marketed Since 2023-09-12
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": "0ce97a26-ec41-4c7a-8198-4850a9dc81f7", "openfda": {"upc": ["0314789136059"], "unii": ["660YQ98I10"], "rxcui": ["1860136", "1860139"], "spl_set_id": ["8281fd53-f77b-42b1-9b90-449a504f5550"], "manufacturer_name": ["Nexus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, GLASS in 1 CARTON (14789-137-05)  / 20 mL in 1 VIAL, GLASS (14789-137-07)", "package_ndc": "14789-137-05", "marketing_start_date": "20230912"}], "brand_name": "Potassium Chloride", "product_id": "14789-137_0ce97a26-ec41-4c7a-8198-4850a9dc81f7", "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": "14789-137", "generic_name": "Potassium Chloride", "labeler_name": "Nexus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "149 mg/mL"}], "application_number": "ANDA217704", "marketing_category": "ANDA", "marketing_start_date": "20230912", "listing_expiration_date": "20261231"}