Fluoxetine - 55111-149-05 - (Fluoxetine)

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Drug Information of Fluoxetine

Product NDC: 55111-149
Proprietary Name: Fluoxetine
Non Proprietary Name: Fluoxetine
Active Ingredient(s): 40    mg/1 & nbsp;   Fluoxetine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Fluoxetine

Product NDC: 55111-149
Labeler Name: Dr.Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075465
Marketing Category: ANDA
Start Marketing Date: 20021015

Package Information of Fluoxetine

Package NDC: 55111-149-05
Package Description: 500 CAPSULE in 1 BOTTLE (55111-149-05)

NDC Information of Fluoxetine

NDC Code 55111-149-05
Proprietary Name Fluoxetine
Package Description 500 CAPSULE in 1 BOTTLE (55111-149-05)
Product NDC 55111-149
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoxetine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20021015
Marketing Category Name ANDA
Labeler Name Dr.Reddy's Laboratories Limited
Substance Name FLUOXETINE HYDROCHLORIDE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Fluoxetine


General Information