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"51662-1678-1" National Drug Code (NDC)
Ondansetron 30 TABLET, FILM COATED in 1 BOTTLE (51662-1678-1)
(HF Acquisition Co LLC, DBA HealthFirst)
NDC Code
51662-1678-1
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (51662-1678-1)
Product NDC
51662-1678
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ondansetron
Non-Proprietary Name
Ondansetron
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20061226
Marketing Category Name
ANDA
Application Number
ANDA076183
Manufacturer
HF Acquisition Co LLC, DBA HealthFirst
Substance Name
ONDANSETRON HYDROCHLORIDE
Strength
4
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/51662-1678-1