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"61919-565-12" National Drug Code (NDC)
Ondansetron 12 TABLET, FILM COATED in 1 BOTTLE (61919-565-12)
(Direct_Rx)
NDC Code
61919-565-12
Package Description
12 TABLET, FILM COATED in 1 BOTTLE (61919-565-12)
Product NDC
61919-565
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ondansetron
Non-Proprietary Name
Ondansetron
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20190906
Marketing Category Name
ANDA
Application Number
ANDA078539
Manufacturer
Direct_Rx
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/61919-565-12