Potassium Chloride

Product NDC

0409-7076

11-digit product format

004097076

Labeler code

0409

Product ID

0409-7076_cad092f3-953f-4130-8d44-7285b2833973

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

0000-00-00

Substance

POTASSIUM CHLORIDE

Active strength

30 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

2020-12-31

Current FDA listing

Historical FDA.report record