potassium chloride

Generic: potassium chloride

Labeler: b. braun medical inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler b. braun medical inc.
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
PARENTERAL
Active Ingredients

potassium chloride 14.9 g/100mL

Manufacturer
B. Braun Medical Inc.

Identifiers & Regulatory

Product NDC 0264-1944
Product ID 0264-1944_95c83840-ae78-4210-8b5f-cf4120989811
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA085870
Listing Expiration 2026-12-31
Marketing Start 2022-05-02

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 02641944
Hyphenated Format 0264-1944

Supplemental Identifiers

RxCUI
204520
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 ANDA085870 (source: ndc)
Routes
PARENTERAL
source: ndc

Resolved Composition

Strengths
  • 14.9 g/100mL
source: ndc
Packaging
  • 24 CONTAINER in 1 CASE (0264-1944-20) / 250 mL in 1 CONTAINER
source: ndc

Packages (1)

Ingredients (1)

potassium chloride (14.9 g/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["PARENTERAL"], "spl_id": "95c83840-ae78-4210-8b5f-cf4120989811", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["204520"], "spl_set_id": ["ab67b151-8368-4321-b562-bad5eff7b740"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 CONTAINER in 1 CASE (0264-1944-20)  / 250 mL in 1 CONTAINER", "package_ndc": "0264-1944-20", "marketing_start_date": "20220502"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "0264-1944_95c83840-ae78-4210-8b5f-cf4120989811", "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": "0264-1944", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "B. Braun Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "14.9 g/100mL"}], "application_number": "ANDA085870", "marketing_category": "ANDA", "marketing_start_date": "20220502", "listing_expiration_date": "20261231"}