Fluoxetine - 51079-971-19 - (fluoxetine hydrochloride)

Alphabetical Index


Drug Information of Fluoxetine

Product NDC: 51079-971
Proprietary Name: Fluoxetine
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

Product NDC: 51079-971
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075207
Marketing Category: ANDA
Start Marketing Date: 20110711

Package Information of Fluoxetine

Package NDC: 51079-971-19
Package Description: 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-971-19) > 1 CAPSULE in 1 BLISTER PACK (51079-971-17)

NDC Information of Fluoxetine

NDC Code 51079-971-19
Proprietary Name Fluoxetine
Package Description 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-971-19) > 1 CAPSULE in 1 BLISTER PACK (51079-971-17)
Product NDC 51079-971
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluoxetine hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110711
Marketing Category Name ANDA
Labeler Name UDL Laboratories, 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


General Information