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Fluoxetine Hydrochloride - 55289-610-28 - (Fluoxetine Hydrochloride)

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Drug Information of Fluoxetine Hydrochloride

Product NDC: 55289-610
Proprietary Name: Fluoxetine Hydrochloride
Non Proprietary Name: Fluoxetine Hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   Fluoxetine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Fluoxetine Hydrochloride

Product NDC: 55289-610
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075049
Marketing Category: ANDA
Start Marketing Date: 20020129

Package Information of Fluoxetine Hydrochloride

Package NDC: 55289-610-28
Package Description: 28 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (55289-610-28) > 14 CAPSULE in 1 BOTTLE, PLASTIC (55289-610-14)

NDC Information of Fluoxetine Hydrochloride

NDC Code 55289-610-28
Proprietary Name Fluoxetine Hydrochloride
Package Description 28 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (55289-610-28) > 14 CAPSULE in 1 BOTTLE, PLASTIC (55289-610-14)
Product NDC 55289-610
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoxetine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20020129
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name FLUOXETINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Fluoxetine Hydrochloride


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