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"53002-1796-3" National Drug Code (NDC)

Fluoxetine Hydrochloride 30 TABLET in 1 BOTTLE (53002-1796-3)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-1796-3
Package Description30 TABLET in 1 BOTTLE (53002-1796-3)
Product NDC53002-1796
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFluoxetine Hydrochloride
Non-Proprietary NameFluoxetine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20190807
Marketing Category NameANDA
Application NumberANDA211653
ManufacturerRPK Pharmaceuticals, Inc.
Substance NameFLUOXETINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/53002-1796-3





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