www.ndcvalidator.com
National Drug Code Lookup | NDC Directory | About | Feedback

"70518-2162-0" National Drug Code (NDC)

Fluoxetine 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2162-0)
(REMEDYREPACK INC.)

NDC Code70518-2162-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2162-0)
Product NDC70518-2162
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFluoxetine
Non-Proprietary NameFluoxetine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190627
Marketing Category NameANDA
Application NumberANDA075755
ManufacturerREMEDYREPACK INC.
Substance NameFLUOXETINE HYDROCHLORIDE
Strength20
Strength Unitmg/1
Pharmacy ClassesSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2162-0





Copyright © 2007-2024 www.ndcvalidator.com