potassium chloride

Product NDC

68084-419

11-digit product format

680840419

Labeler code

68084

Product ID

68084-419_66d7a970-d12f-7c88-e053-2a91aa0a9c66

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

potassium chloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

American Health Packaging

Application

NDA018238

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2012-06-26

Marketing end

2019-08-31

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

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record