Potassium Chloride

Product NDC

0338-0707

11-digit product format

003380707

Labeler code

0338

Product ID

0338-0707_f9952bbd-8532-4ded-a3a4-08f1f50400b0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

POTASSIUM CHLORIDE

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Baxter Healthcare Corpora

Application

NDA019904

Marketing category

NDA

Marketing start

1989-12-26

Marketing end

0000-00-00

Substance

POTASSIUM CHLOR

Active strength

22 g/1000mL

Pharmacologic classes

Potassium Compo

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record