Potassium Chloride in Dextrose

Product NDC

0409-7996

11-digit product format

004097996

Labeler code

0409

Product ID

0409-7996_5c1443d9-92a9-4c8d-9886-0ce803da5d68

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

DEXTROSE MONOHYDRATE and POTASSIUM CHLORIDE

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Hospira, Inc.

Application

NDA018371

Marketing category

NDA

Marketing start

1980-05-29

Marketing end

0000-00-00

Substance

DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE

Active strength

5 g/100mL; g/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