potassium chloride

Generic: potassium chloride

Labeler: henry schein, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler henry schein, inc.
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

potassium chloride 2 meq/mL

Manufacturer
Henry Schein, Inc.

Identifiers & Regulatory

Product NDC 0404-9936
Product ID 0404-9936_86d210da-05db-45c6-b2fd-4d6aa79484fa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA088901
Listing Expiration 2026-12-31
Marketing Start 2022-01-13

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 04049936
Hyphenated Format 0404-9936

Supplemental Identifiers

RxCUI
1860132 1860139
UNII
660YQ98I10

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 ANDA088901 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2 meq/mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9936-10) / 5 mL in 1 VIAL, SINGLE-DOSE
  • 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9936-20) / 20 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (2)

0404-9936-10 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9936-10) / 5 mL in 1 VIAL, SINGLE-DOSE 0404-9936-20 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9936-20) / 20 mL in 1 VIAL, SINGLE-DOSE

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": "86d210da-05db-45c6-b2fd-4d6aa79484fa", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1860132", "1860139"], "spl_set_id": ["bf8e8ac7-e6a8-4571-a0ea-7bcab89290f6"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9936-10)  / 5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9936-10", "marketing_start_date": "20220113"}, {"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9936-20)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9936-20", "marketing_start_date": "20220113"}], "brand_name": "Potassium Chloride", "product_id": "0404-9936_86d210da-05db-45c6-b2fd-4d6aa79484fa", "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": "0404-9936", "generic_name": "Potassium Chloride", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "2 meq/mL"}], "application_number": "ANDA088901", "marketing_category": "ANDA", "marketing_start_date": "20220113", "listing_expiration_date": "20261231"}