potassium chloride in sodium chloride (0990-9257)

Drug Facts

Product Profile

Brand Name potassium chloride in sodium chloride

Generic Name sodium chloride and potassium chloride

Labeler icu medical inc.

Dosage Form INJECTION, SOLUTION

Routes

INTRAVENOUS

Active Ingredients

potassium chloride 1.49 g/1000mL, sodium chloride 4.5 g/1000mL

Manufacturer

ICU Medical Inc.

Identifiers & Regulatory

Product NDC 0990-9257

Product ID 0990-9257_75d665b8-1e91-436f-86f6-ca8d284ab438

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA078446

Listing Expiration 2026-12-31

Marketing Start 2020-01-01

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 09909257

Hyphenated Format 0990-9257

Supplemental Identifiers

RxCUI

403890

UNII

660YQ98I10 451W47IQ8X

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 sodium chloride (source: ndc)

Generic Name sodium chloride and potassium chloride (source: ndc)

Application Number ANDA078446 (source: ndc)

Routes

INTRAVENOUS

source: ndc

Resolved Composition

Strengths

1.49 g/1000mL
4.5 g/1000mL

source: ndc

Packaging

12 POUCH in 1 CASE (0990-9257-39) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG

source: ndc

Packages (1)

0990-9257-39 12 POUCH in 1 CASE (0990-9257-39) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG

Ingredients (2)

potassium chloride (1.49 g/1000mL) sodium chloride (4.5 g/1000mL)

Linked Drug Pages (1)

Potassium Chloride in Sodium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["INTRAVENOUS"], "spl_id": "75d665b8-1e91-436f-86f6-ca8d284ab438", "openfda": {"unii": ["660YQ98I10", "451W47IQ8X"], "rxcui": ["403890"], "spl_set_id": ["243fe8fc-996a-4855-8daf-069628e547c4"], "manufacturer_name": ["ICU Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 POUCH in 1 CASE (0990-9257-39)  / 1 BAG in 1 POUCH / 1000 mL in 1 BAG", "package_ndc": "0990-9257-39", "marketing_start_date": "20200301"}], "brand_name": "Potassium Chloride in Sodium Chloride", "product_id": "0990-9257_75d665b8-1e91-436f-86f6-ca8d284ab438", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0990-9257", "generic_name": "SODIUM CHLORIDE and POTASSIUM CHLORIDE", "labeler_name": "ICU Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride in Sodium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.49 g/1000mL"}, {"name": "SODIUM CHLORIDE", "strength": "4.5 g/1000mL"}], "application_number": "ANDA078446", "marketing_category": "ANDA", "marketing_start_date": "20200101", "listing_expiration_date": "20261231"}