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"61919-087-20" National Drug Code (NDC)

Ondansetron 20 TABLET, FILM COATED in 1 BOTTLE (61919-087-20)
(DIRECT RX)

NDC Code61919-087-20
Package Description20 TABLET, FILM COATED in 1 BOTTLE (61919-087-20)
Product NDC61919-087
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOndansetron
Non-Proprietary NameOndansetron
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170310
Marketing Category NameANDA
Application NumberANDA078539
ManufacturerDIRECT RX
Substance NameONDANSETRON HYDROCHLORIDE
Strength8
Strength Unitmg/1
Pharmacy ClassesSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-087-20





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