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"70518-2337-0" National Drug Code (NDC)

Olanzapine 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2337-0)
(REMEDYREPACK INC.)

NDC Code70518-2337-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2337-0)
Product NDC70518-2337
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOlanzapine
Non-Proprietary NameOlanzapine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20191002
Marketing Category NameANDA
Application NumberANDA202862
ManufacturerREMEDYREPACK INC.
Substance NameOLANZAPINE
Strength20
Strength Unitmg/1
Pharmacy ClassesAtypical Antipsychotic [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2337-0





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