Fluoxetine - 21695-054-90 - (fluoxetine)

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Drug Information of Fluoxetine

Product NDC: 21695-054
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: 21695-054
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076990
Marketing Category: ANDA
Start Marketing Date: 20050720

Package Information of Fluoxetine

Package NDC: 21695-054-90
Package Description: 90 CAPSULE in 1 BOTTLE (21695-054-90)

NDC Information of Fluoxetine

NDC Code 21695-054-90
Proprietary Name Fluoxetine
Package Description 90 CAPSULE in 1 BOTTLE (21695-054-90)
Product NDC 21695-054
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluoxetine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20050720
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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