Potassium Chloride

Product NDC

60687-310

11-digit product format

606870310

Labeler code

60687

Product ID

60687-310_a693d0c5-c37e-0c0d-e053-2a95a90afb49

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Potassium Chloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

American Health Packaging

Application

ANDA202128

Marketing category

ANDA

Marketing start

2017-11-13

Marketing end

2021-01-31

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