Package 51662-1421-1

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 51662-1421-1
Digits Only 5166214211
Product NDC 51662-1421
Product ID 51662-1421_2b37da71-040f-2c5f-e063-6394a90a4194
Description

20 mL in 1 VIAL, SINGLE-DOSE (51662-1421-1)

Marketing

Marketing Status
Marketed Since 2019-10-18
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": "2b37da71-040f-2c5f-e063-6394a90a4194", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1860139"], "spl_set_id": ["951ffdc3-d54f-d5e1-e053-2a95a90a79e6"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL, SINGLE-DOSE (51662-1421-1)", "package_ndc": "51662-1421-1", "marketing_start_date": "20191018"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "51662-1421_2b37da71-040f-2c5f-e063-6394a90a4194", "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": "51662-1421", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "149 mg/mL"}], "application_number": "ANDA080205", "marketing_category": "ANDA", "marketing_start_date": "20191018", "listing_expiration_date": "20261231"}