"61786-699-02" National Drug Code (NDC)

Ondansetron Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (61786-699-02)
(REMEDYREPACK INC.)

NDC Code61786-699-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (61786-699-02)
Product NDC61786-699
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOndansetron Hydrochloride
Non-Proprietary NameOndansetron Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160519
Marketing Category NameANDA
Application NumberANDA077050
ManufacturerREMEDYREPACK INC.
Substance NameONDANSETRON HYDROCHLORIDE
Strength8
Strength Unitmg/1
Pharmacy ClassesSerotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

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