"71930-018-52" National Drug Code (NDC)

Ondansetron 500 TABLET in 1 BOTTLE (71930-018-52)
(Eywa Pharma Inc.)

NDC Code71930-018-52
Package Description500 TABLET in 1 BOTTLE (71930-018-52)
Product NDC71930-018
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOndansetron
Non-Proprietary NameOndansetron
Dosage FormTABLET
UsageORAL
Start Marketing Date20180711
Marketing Category NameANDA
Application NumberANDA077851
ManufacturerEywa Pharma Inc.
Substance NameONDANSETRON HYDROCHLORIDE
Strength8
Strength Unitmg/1
Pharmacy ClassesSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]

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