potassium chloride

Generic: potassium chloride

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

potassium chloride 149 mg/mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-6653
Product ID 0409-6653_51305788-d1bb-4fef-86a7-6e62f7b01f00
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA080205
Listing Expiration 2027-12-31
Marketing Start 2005-08-08

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 04096653
Hyphenated Format 0409-6653

Supplemental Identifiers

RxCUI
1860132 1860136 1860139
UNII
660YQ98I10

Packaging Origin

Original Packager
true

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
  • 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6653-05) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-6653-18)
source: ndc

Packages (1)

0409-6653-05 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6653-05) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-6653-18)

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": "51305788-d1bb-4fef-86a7-6e62f7b01f00", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1860132", "1860136", "1860139"], "spl_set_id": ["559a0a8c-a8fe-40a5-b196-21f9308780ab"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6653-05)  / 20 mL in 1 VIAL, SINGLE-DOSE (0409-6653-18)", "package_ndc": "0409-6653-05", "marketing_start_date": "20050808"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "0409-6653_51305788-d1bb-4fef-86a7-6e62f7b01f00", "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": "0409-6653", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Hospira, Inc.", "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": "20050808", "listing_expiration_date": "20271231"}