MedPath

Potassium Chloride for Oral Solution

These highlights do not include all the information needed to use POTASSIUM CHLORIDE FOR ORAL SOLUTION safely and effectively. See full prescribing information for POTASSIUM CHLORIDE FOR ORAL SOLUTION. POTASSIUM CHLORIDE for oral solution Initial U.S. Approval: 1948

Approved
Approval ID

0e4fd822-9167-4451-b8fe-9a63e09f7ed1

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Oct 5, 2023

Manufacturers
FDA

Belcher Pharmaceuticals LLC

DUNS: 965082543

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Potassium Chloride for Oral Solution

PRODUCT DETAILS

NDC Product Code62250-690
Application NumberANDA212183
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateOctober 5, 2023
Generic NamePotassium Chloride for Oral Solution

INGREDIENTS (6)

ANHYDROUS CITRIC ACIDInactive
Code: XF417D3PSL
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
SUCRALOSEInactive
Code: 96K6UQ3ZD4
Classification: IACT
POTASSIUM CHLORIDEActive
Quantity: 1.5 g in 1.58 g
Code: 660YQ98I10
Classification: ACTIB
ORANGEInactive
Code: 5EVU04N5QU
Classification: IACT
FD&C YELLOW NO. 6Inactive
Code: H77VEI93A8
Classification: IACT

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Potassium Chloride for Oral Solution - FDA Drug Approval Details