Potassium Chloride

Product NDC

63739-446

11-digit product format

637390446

Labeler code

63739

Product ID

63739-446_e3deb79f-888c-4ebc-8b30-c5256d2b9a06

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Potassium Chloride

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

McKesson Packaging Services Business Unit of McKesson Corporation

Application

ANDA074726

Marketing category

ANDA

Marketing start

2009-08-03

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