potassium chloride

Generic: potassium chloride

Labeler: icu medical inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

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

potassium chloride 400 meq/1000mL

Manufacturer
ICU Medical Inc.

Identifiers & Regulatory

Product NDC 0990-7077
Product ID 0990-7077_88bcbbe4-9ebf-4491-874a-c4c4c7f1f90d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020161
Listing Expiration 2026-12-31
Marketing Start 2019-04-01

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 09907077
Hyphenated Format 0990-7077

Supplemental Identifiers

RxCUI
312507 1860239 1860241 1860463 1860466
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 NDA020161 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 400 meq/1000mL
source: ndc
Packaging
  • 24 POUCH in 1 CASE (0990-7077-14) / 1 BAG in 1 POUCH / 50 mL in 1 BAG
  • 24 POUCH in 1 CASE (0990-7077-26) / 1 BAG in 1 POUCH / 100 mL in 1 BAG
source: ndc

Packages (2)

0990-7077-14 24 POUCH in 1 CASE (0990-7077-14) / 1 BAG in 1 POUCH / 50 mL in 1 BAG 0990-7077-26 24 POUCH in 1 CASE (0990-7077-26) / 1 BAG in 1 POUCH / 100 mL in 1 BAG

Ingredients (1)

potassium chloride (400 meq/1000mL)

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "88bcbbe4-9ebf-4491-874a-c4c4c7f1f90d", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312507", "1860239", "1860241", "1860463", "1860466"], "spl_set_id": ["eb56a807-ea94-4edb-9811-a04b19568468"], "manufacturer_name": ["ICU Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 POUCH in 1 CASE (0990-7077-14)  / 1 BAG in 1 POUCH / 50 mL in 1 BAG", "package_ndc": "0990-7077-14", "marketing_start_date": "20190601"}, {"sample": false, "description": "24 POUCH in 1 CASE (0990-7077-26)  / 1 BAG in 1 POUCH / 100 mL in 1 BAG", "package_ndc": "0990-7077-26", "marketing_start_date": "20191231"}], "brand_name": "Potassium Chloride", "product_id": "0990-7077_88bcbbe4-9ebf-4491-874a-c4c4c7f1f90d", "dosage_form": "INJECTION, SOLUTION", "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": "0990-7077", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "ICU Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "400 meq/1000mL"}], "application_number": "NDA020161", "marketing_category": "NDA", "marketing_start_date": "20190401", "listing_expiration_date": "20261231"}