Ondansetron Hydrochloride

Product NDC
23155-168
11-digit product format
231550168
Labeler code
23155
Product ID
23155-168_ad6dc125-1b99-4e50-ac4f-eca143164f41
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ondansetron Hydrochloride
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
Heritage Pharmaceuticals Inc.
Application
ANDA090424
Marketing category
ANDA
Marketing start
2012-12-13
Marketing end
0000-00-00
Substance
ONDANSETRON HYDROCHLORIDE
Active strength
2 mg/mL
Pharmacologic classes
Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
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
23155-168-31ML - Milliliter23155-1684f5ac2b1-e829-45ed-b860-786d4a9c779212013-02-13