Potassium Chloride in Sodium Chloride

Product NDC

0409-7115

11-digit product format

004097115

Labeler code

0409

Product ID

0409-7115_59e7efc7-7c2b-41db-a637-31ba7c7f4aa1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

SODIUM CHLORIDE and POTASSIUM CHLORIDE

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Hospira, Inc.

Application

NDA019686

Marketing category

NDA

Marketing start

1988-10-17

Marketing end

2020-09-01

Substance

SODIUM CHLORIDE; POTASSIUM CHLORIDE

Active strength

9 g/1000mL; g/1000mL

Pharmacologic classes

Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],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