potassium chloride in dextrose (0990-7905)

Drug Facts

Product Profile

Brand Name potassium chloride in dextrose

Generic Name dextrose monohydrate and potassium chloride injection, solution

Labeler icu medical inc.

Dosage Form INJECTION, SOLUTION

Routes

INTRAVENOUS

Active Ingredients

dextrose monohydrate 5 g/100mL, potassium chloride .149 g/100mL

Manufacturer

ICU Medical Inc.

Identifiers & Regulatory

Product NDC 0990-7905

Product ID 0990-7905_357fc68c-2f4c-4f4c-9e26-a66ff54c59ff

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category NDA

Application Number NDA018371

Listing Expiration 2026-12-31

Marketing Start 2020-11-20

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 09907905

Hyphenated Format 0990-7905

Supplemental Identifiers

RxCUI

309783

UNII

LX22YL083G 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 in dextrose (source: ndc)

Generic Name dextrose monohydrate and potassium chloride injection, solution (source: ndc)

Application Number NDA018371 (source: ndc)

Routes

INTRAVENOUS

source: ndc

Resolved Composition

Strengths

5 g/100mL
.149 g/100mL

source: ndc

Packaging

12 POUCH in 1 CASE (0990-7905-09) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG

source: ndc

Packages (1)

0990-7905-09 12 POUCH in 1 CASE (0990-7905-09) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG

Ingredients (2)

dextrose monohydrate (5 g/100mL) potassium chloride (.149 g/100mL)

Linked Drug Pages (1)

Potassium Chloride in Dextrose ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["INTRAVENOUS"], "spl_id": "357fc68c-2f4c-4f4c-9e26-a66ff54c59ff", "openfda": {"unii": ["LX22YL083G", "660YQ98I10"], "rxcui": ["309783"], "spl_set_id": ["02d694b5-3600-4d55-bd5c-924abaec5315"], "manufacturer_name": ["ICU Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 POUCH in 1 CASE (0990-7905-09)  / 1 BAG in 1 POUCH / 1000 mL in 1 BAG", "package_ndc": "0990-7905-09", "marketing_start_date": "20201120"}], "brand_name": "Potassium Chloride in Dextrose", "product_id": "0990-7905_357fc68c-2f4c-4f4c-9e26-a66ff54c59ff", "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": "0990-7905", "generic_name": "dextrose monohydrate and potassium chloride injection, solution", "labeler_name": "ICU Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride in Dextrose", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5 g/100mL"}, {"name": "POTASSIUM CHLORIDE", "strength": ".149 g/100mL"}], "application_number": "NDA018371", "marketing_category": "NDA", "marketing_start_date": "20201120", "listing_expiration_date": "20261231"}