Fluoxetine - 0121-4721-05 - (FLUOXETINE HYDROCHLORIDE)

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Drug Information of Fluoxetine

Product NDC: 0121-4721
Proprietary Name: Fluoxetine
Non Proprietary Name: FLUOXETINE HYDROCHLORIDE
Active Ingredient(s): 20    mg/5mL & nbsp;   FLUOXETINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fluoxetine

Product NDC: 0121-4721
Labeler Name: Pharmaceutical Associates, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076015
Marketing Category: ANDA
Start Marketing Date: 20020201

Package Information of Fluoxetine

Package NDC: 0121-4721-05
Package Description: 5 mL in 1 CUP, UNIT-DOSE (0121-4721-05)

NDC Information of Fluoxetine

NDC Code 0121-4721-05
Proprietary Name Fluoxetine
Package Description 5 mL in 1 CUP, UNIT-DOSE (0121-4721-05)
Product NDC 0121-4721
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FLUOXETINE HYDROCHLORIDE
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20020201
Marketing Category Name ANDA
Labeler Name Pharmaceutical Associates, Inc.
Substance Name FLUOXETINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/5mL
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Fluoxetine


General Information