HESPAN

Product NDC
0264-1965
11-digit product format
002641965
Labeler code
0264
Product ID
0264-1965_47e5d437-857d-4328-bdda-e6ff01544d9d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hetastarch in Sodium Chloride
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
B. Braun Medical Inc.
Application
BN890105
Marketing category
NDA
Marketing start
1991-04-04
Marketing end
0000-00-00
Substance
HETASTARCH; SODIUM CHLORIDE
Active strength
6 g/100mL; g/100mL
Pharmacologic classes
Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Plasma Volume Expander [EPC],Increased Intravascular Volume [PE],Osmotic Activity [MoA],Starch [CS]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0264-1965-10ML - Milliliter0264-1965d87fc720-b395-4f0c-aa1b-cd42cb9c2c1f12012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0264-1965-100026419651012 CONTAINER in 1 CASE (0264-1965-10) > 500 mL in 1 CONTAINER12 container1991-04-040000-00-00NoNoCurrent