ondansetron

Product NDC
50090-1600
11-digit product format
500901600
Labeler code
50090
Product ID
50090-1600_fd594d7c-490d-4257-aa3e-1a28f8215b94
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ondansetron hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA077851
Marketing category
ANDA
Marketing start
2007-06-25
Marketing end
0000-00-00
Substance
ONDANSETRON HYDROCHLORIDE
Active strength
4 mg/1
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
50090-1600-0EA - Each50090-1600e6eb906e-e1d5-4ccb-8e79-76678320961812018-11-06
50090-1600-1EA - Each50090-1600528a836b-4b9c-4785-b6f2-08eeb4bced9112018-11-06
50090-1600-2EA - Each50090-1600644e41c9-5171-4805-b5fa-21f1584e028112018-11-06
50090-1600-4EA - Each50090-160092ff04e7-8209-41f2-8e07-14d68bfb644612018-08-13
50090-1600-5EA - Each50090-16009a9427e4-8b2d-4ab0-bfcd-a544e0485ad412018-11-06