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"42708-059-05" National Drug Code (NDC)
Ondansetron Hydrochloride 5 TABLET, FILM COATED in 1 BOTTLE (42708-059-05)
(QPharma Inc)
NDC Code
42708-059-05
Package Description
5 TABLET, FILM COATED in 1 BOTTLE (42708-059-05)
Product NDC
42708-059
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ondansetron Hydrochloride
Non-Proprietary Name
Ondansetron Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20070731
Marketing Category Name
ANDA
Application Number
ANDA078539
Manufacturer
QPharma Inc
Substance Name
ONDANSETRON HYDROCHLORIDE
Strength
8
Strength Unit
mg/1
Pharmacy Classes
Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/42708-059-05