"61919-565-20" National Drug Code (NDC)

Ondansetron 20 TABLET, FILM COATED in 1 BOTTLE (61919-565-20)
(DIRECT RX)

NDC Code61919-565-20
Package Description20 TABLET, FILM COATED in 1 BOTTLE (61919-565-20)
Product NDC61919-565
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOndansetron
Non-Proprietary NameOndansetron
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160323
Marketing Category NameANDA
Application NumberANDA078539
ManufacturerDIRECT RX
Substance NameONDANSETRON HYDROCHLORIDE
Strength4
Strength Unitmg/1
Pharmacy ClassesSerotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

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