Potassium Chloride

Product NDC

10370-220

11-digit product format

103700220

Labeler code

10370

Product ID

10370-220_4f4bc944-e9f3-46bf-919e-0bdd4bb9b34a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Potassium Chloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

Par Pharmaceutical, Inc.

Application

ANDA202886

Marketing category

ANDA

Marketing start

2013-12-26

Marketing end

2020-01-31

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

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record