Potassium Chloride

Product NDC

0904-6507

11-digit product format

009046507

Labeler code

0904

Product ID

0904-6507_084de6dc-7339-48de-a2fd-a14410026483

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Potassium Chloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Major Pharmaceuticals

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