Potassium Chloride

Product NDC

50090-2113

11-digit product format

500902113

Labeler code

50090

Product ID

50090-2113_96513be3-8a82-4185-b3dc-44dd5dd30c08

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Potassium Chloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

A-S Medication Solutions

Application

NDA018279

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2014-01-16

Marketing end

0000-00-00

Substance

POTASSIUM CHLORIDE

Active strength

1500 mg/1

Pharmacologic classes

Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record