potassium chloride

Generic: potassium chloride, dextrose monohydrate

Labeler: fresenius kabi usa, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride, dextrose monohydrate
Labeler fresenius kabi usa, llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

dextrose monohydrate 5 g/100mL, potassium chloride 75 mg/100mL

Manufacturer
Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 63323-667
Product ID 63323-667_fa0a4b99-d041-42d8-843d-e7dbead01d89
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212346
Listing Expiration 2026-12-31
Marketing Start 2021-04-23

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 63323667
Hyphenated Format 63323-667

Supplemental Identifiers

RxCUI
309783 2566844
UNII
660YQ98I10 LX22YL083G

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, dextrose monohydrate (source: ndc)
Application Number ANDA212346 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 g/100mL
  • 75 mg/100mL
source: ndc
Packaging
  • 10 BAG in 1 CASE (63323-667-10) / 1000 mL in 1 BAG (63323-667-01)
source: ndc

Packages (1)

63323-667-10 10 BAG in 1 CASE (63323-667-10) / 1000 mL in 1 BAG (63323-667-01)

Ingredients (2)

dextrose monohydrate (5 g/100mL) potassium chloride (75 mg/100mL)

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "fa0a4b99-d041-42d8-843d-e7dbead01d89", "openfda": {"unii": ["660YQ98I10", "LX22YL083G"], "rxcui": ["309783", "2566844"], "spl_set_id": ["55d9ae37-4553-47e7-a2e3-86b48b5227cd"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BAG in 1 CASE (63323-667-10)  / 1000 mL in 1 BAG (63323-667-01)", "package_ndc": "63323-667-10", "marketing_start_date": "20210423"}], "brand_name": "Potassium Chloride", "product_id": "63323-667_fa0a4b99-d041-42d8-843d-e7dbead01d89", "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": "63323-667", "generic_name": "Potassium Chloride, Dextrose Monohydrate", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5 g/100mL"}, {"name": "POTASSIUM CHLORIDE", "strength": "75 mg/100mL"}], "application_number": "ANDA212346", "marketing_category": "ANDA", "marketing_start_date": "20210423", "listing_expiration_date": "20261231"}