ONDANSETRON

Product NDC
55700-064
11-digit product format
557000064
Labeler code
55700
Product ID
55700-064_cdbf69a3-d5f4-4b96-bd16-53a491c0c4b4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ONDANSETRON
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA077851
Marketing category
ANDA
Marketing start
2007-06-25
Marketing end
0000-00-00
Substance
ONDANSETRON HYDROCHLORIDE
Active strength
8 mg/1
Pharmacologic classes
Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-064-06EA - Each55700-0645a5e0eb8-747f-495d-bea2-29ba919f99a512017-03-06
55700-064-10EA - Each55700-064fce3b8a7-8115-4372-9335-47f25575bc4f12017-03-06
55700-064-12EA - Each55700-064d89e6593-0166-4930-bec1-63e195ce1f4612015-04-03
55700-064-20EA - Each55700-0643a0f432d-2736-4580-ae59-48176df1cc4012015-04-03
55700-064-30EA - Each55700-064fcf9972b-b39e-4bcf-bc81-ad20e988096812015-04-03