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 149 mg/mL

Manufacturer
Henry Schein, Inc.

Identifiers & Regulatory

Product NDC 0404-9937
Product ID 0404-9937_b10f2db5-f661-422e-b335-a9c2914aa69d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA080205
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 04049937
Hyphenated Format 0404-9937

Supplemental Identifiers

RxCUI
1860136
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 ANDA080205 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 149 mg/mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9937-10) / 1 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

Ingredients (1)

potassium chloride (149 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b10f2db5-f661-422e-b335-a9c2914aa69d", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1860136"], "spl_set_id": ["8367a2ae-dfd9-4515-838c-529920291ca0"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9937-10)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9937-10", "marketing_start_date": "20220113"}], "brand_name": "Potassium Chloride", "product_id": "0404-9937_b10f2db5-f661-422e-b335-a9c2914aa69d", "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": "0404-9937", "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": "149 mg/mL"}], "application_number": "ANDA080205", "marketing_category": "ANDA", "marketing_start_date": "20220113", "listing_expiration_date": "20261231"}