Potassium Chloride in Sodium Chloride

Product NDC

0409-9257

11-digit product format

004099257

Labeler code

0409

Product ID

0409-9257_45c67f81-8540-4f22-a4e9-7c12d159d5bd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

SODIUM CHLORIDE and POTASSIUM CHLORIDE

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Hospira, Inc.

Application

ANDA078446

Marketing category

ANDA

Marketing start

2008-12-05

Marketing end

2020-09-01

Substance

SODIUM CHLORIDE; POTASSIUM CHLORIDE

Active strength

5 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