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
Routes
INTRAVENOUS
Active Ingredients

potassium chloride 20 meq/50mL

Manufacturer
Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 65219-008
Product ID 65219-008_771b8cdf-5287-4678-af79-7dc0c78245cc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211087
Listing Expiration 2026-12-31
Marketing Start 2021-06-25

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 65219008
Hyphenated Format 65219-008

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 ANDA211087 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 meq/50mL
source: ndc
Packaging
  • 60 BAG in 1 CARTON (65219-008-51) / 50 mL in 1 BAG (65219-008-50)
source: ndc

Packages (1)

65219-008-51 60 BAG in 1 CARTON (65219-008-51) / 50 mL in 1 BAG (65219-008-50)

Ingredients (1)

potassium chloride (20 meq/50mL)

Linked Drug Pages (1)

POTASSIUM CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "771b8cdf-5287-4678-af79-7dc0c78245cc", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312507", "1860239", "1860241", "1860463", "1860466"], "spl_set_id": ["3849b89c-c309-46fb-a1e2-53ff0c65077f"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 BAG in 1 CARTON (65219-008-51)  / 50 mL in 1 BAG (65219-008-50)", "package_ndc": "65219-008-51", "marketing_start_date": "20210625"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "65219-008_771b8cdf-5287-4678-af79-7dc0c78245cc", "dosage_form": "INJECTION", "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": "65219-008", "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": "20 meq/50mL"}], "application_number": "ANDA211087", "marketing_category": "ANDA", "marketing_start_date": "20210625", "listing_expiration_date": "20261231"}