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"55111-284-48" National Drug Code (NDC)

Fluoxetine Hydrochloride 1 BLISTER PACK in 1 CARTON (55111-284-48) / 4 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK
(Dr.Reddy's Laboratories Limited)

NDC Code55111-284-48
Package Description1 BLISTER PACK in 1 CARTON (55111-284-48) / 4 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK
Product NDC55111-284
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFluoxetine Hydrochloride
Non-Proprietary NameFluoxetine Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE PELLETS
UsageORAL
Start Marketing Date20100324
Marketing Category NameANDA
Application NumberANDA078572
ManufacturerDr.Reddy's Laboratories Limited
Substance NameFLUOXETINE HYDROCHLORIDE
Strength90
Strength Unitmg/1
Pharmacy ClassesSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]

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