potassium chloride

Generic: potassium chloride

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
Labeler fresenius kabi usa, llc
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

potassium chloride 2 meq/mL

Manufacturer
Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 63323-967
Product ID 63323-967_a1b31b46-2bb4-457e-a30b-e7dab47a2c54
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA088908
Listing Expiration 2026-12-31
Marketing Start 2000-09-05

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 63323967
Hyphenated Format 63323-967

Supplemental Identifiers

RxCUI
204520 1860132 1860136 1860139
UPC
0363323967017 0363323965020 0363323965013
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 ANDA088908 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2 meq/mL
source: ndc
Packaging
  • 25 VIAL, MULTI-DOSE in 1 TRAY (63323-967-30) / 30 mL in 1 VIAL, MULTI-DOSE (63323-967-01)
source: ndc

Packages (1)

63323-967-30 25 VIAL, MULTI-DOSE in 1 TRAY (63323-967-30) / 30 mL in 1 VIAL, MULTI-DOSE (63323-967-01)

Ingredients (1)

potassium chloride (2 meq/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": "a1b31b46-2bb4-457e-a30b-e7dab47a2c54", "openfda": {"upc": ["0363323967017", "0363323965020", "0363323965013"], "unii": ["660YQ98I10"], "rxcui": ["204520", "1860132", "1860136", "1860139"], "spl_set_id": ["fcd4f458-ce27-417e-9bb6-de1cc49d44b9"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 TRAY (63323-967-30)  / 30 mL in 1 VIAL, MULTI-DOSE (63323-967-01)", "package_ndc": "63323-967-30", "marketing_start_date": "20000905"}], "brand_name": "Potassium Chloride", "product_id": "63323-967_a1b31b46-2bb4-457e-a30b-e7dab47a2c54", "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": "63323-967", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "2 meq/mL"}], "application_number": "ANDA088908", "marketing_category": "ANDA", "marketing_start_date": "20000905", "listing_expiration_date": "20261231"}