Potassium Chloride in Dextrose and Sodium Chloride

Product NDC

0409-7998

11-digit product format

004097998

Labeler code

0409

Product ID

0409-7998_0b7cb442-ad52-4c4e-b432-9416bb54814d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Hospira, Inc.

Application

NDA018876

Marketing category

NDA

Marketing start

2005-02-28

Marketing end

0000-00-00

Substance

DEXTROSE MONOHYDRATE; SODIUM CHLORIDE; POTASSIUM CHLORIDE

Active strength

50 g/1000mL; 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

2019-12-31

Current FDA listing

Historical FDA.report record