Potassium Chloride

Product NDC

0615-7867

11-digit product format

006157867

Labeler code

0615

Product ID

0615-7867_dfb286b1-ce07-47e4-b62d-04e97d056d42

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

potassium chloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA204662

Marketing category

ANDA

Marketing start

2014-08-21

Marketing end

0000-00-00

Substance

POTASSIUM CHLORIDE

Active strength

10 meq/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