Potassium Chloride

Product NDC

63629-2937

11-digit product format

636292937

Labeler code

63629

Product ID

63629-2937_86987ac1-6359-40c3-b26a-abfa68b3135f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Potassium Chloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

NDA019123

Marketing category

NDA

Marketing start

1986-04-17

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record