potassium chloride

Product NDC

0615-7646

11-digit product format

006157646

Labeler code

0615

Product ID

0615-7646_d2518f4d-eafc-4107-ba76-5453bb220927

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

potassium chloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

NDA018238

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2010-10-25

Marketing end

0000-00-00

Substance

POTASSIUM CHLORIDE

Active strength

750 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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record