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"49884-735-01" National Drug Code (NDC)

Fluoxetine Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49884-735-01)
(Par Pharmaceutical, Inc)

NDC Code49884-735-01
Package Description100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49884-735-01)
Product NDC49884-735
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFluoxetine Hydrochloride
Non-Proprietary NameFluoxetine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20010802
End Marketing Date20161231
Marketing Category NameANDA
Application NumberANDA075755
ManufacturerPar Pharmaceutical, 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/49884-735-01





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