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"51672-5306-2" National Drug Code (NDC)

Fluoxetine Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (51672-5306-2)
(Taro Pharmaceuticals U.S.A., Inc.)

NDC Code51672-5306-2
Package Description500 TABLET, FILM COATED in 1 BOTTLE (51672-5306-2)
Product NDC51672-5306
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFluoxetine Hydrochloride
Non-Proprietary NameFluoxetine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190215
Marketing Category NameANDA
Application NumberANDA211477
ManufacturerTaro Pharmaceuticals U.S.A., Inc.
Substance NameFLUOXETINE HYDROCHLORIDE
Strength60
Strength Unitmg/1
Pharmacy ClassesSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51672-5306-2





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