Potassium Chloride

Product NDC

0409-7074

11-digit product format

004097074

Labeler code

0409

Product ID

0409-7074_66ef4ab7-05d9-4ba0-a8a4-b9d2c09b5c7b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

POTASSIUM CHLORIDE

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Hospira, Inc.

Application

NDA020161

Marketing category

NDA

Marketing start

1992-11-30

Marketing end

2020-09-01

Substance

POTASSIUM CHLORIDE

Active strength

10 meq/100mL

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