potassium chloride

Generic: potassium chloride

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

potassium chloride 149 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1421
Product ID 51662-1421_2b37da71-040f-2c5f-e063-6394a90a4194
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA080205
Listing Expiration 2026-12-31
Marketing Start 2019-10-18

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc] potassium compounds [cs] potassium salt [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621421
Hyphenated Format 51662-1421

Supplemental Identifiers

RxCUI
1860139
UNII
660YQ98I10

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name potassium chloride (source: ndc)
Generic Name potassium chloride (source: ndc)
Application Number ANDA080205 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 149 mg/mL
source: ndc
Packaging
  • 20 mL in 1 VIAL, SINGLE-DOSE (51662-1421-1)
source: ndc

Packages (1)

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

Ingredients (1)

potassium chloride (149 mg/mL)

Linked Drug Pages (1)

POTASSIUM CHLORIDE ndc-match (0.9)

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"}