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"52125-870-02" National Drug Code (NDC)

Ondansetron Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-870-02)
(REMEDYREPACK INC.)

NDC Code52125-870-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (52125-870-02)
Product NDC52125-870
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOndansetron Hydrochloride
Non-Proprietary NameOndansetron Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140311
Marketing Category NameANDA
Application NumberANDA077050
ManufacturerREMEDYREPACK INC.
Substance NameONDANSETRON HYDROCHLORIDE
Strength4
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/52125-870-02





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