Potassium Chloride in Dextrose

Product NDC
0409-7906
11-digit product format
004097906
Labeler code
0409
Product ID
0409-7906_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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0409-7906-09ML - Milliliter0409-7906542af8ee-1108-4cf3-8d10-5bc727a3f6b712012-07-24