Home > National Drug Code (NDC) > Venlafaxine Hydrochloride

Venlafaxine Hydrochloride - 51079-482-20 - (venlafaxine hydrochloride)

Alphabetical Index


Drug Information of Venlafaxine Hydrochloride

Product NDC: 51079-482
Proprietary Name: Venlafaxine Hydrochloride
Non Proprietary Name: venlafaxine hydrochloride
Active Ingredient(s): 75    mg/1 & nbsp;   venlafaxine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Venlafaxine Hydrochloride

Product NDC: 51079-482
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077166
Marketing Category: ANDA
Start Marketing Date: 20120921

Package Information of Venlafaxine Hydrochloride

Package NDC: 51079-482-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-482-20) > 1 TABLET in 1 BLISTER PACK (51079-482-01)

NDC Information of Venlafaxine Hydrochloride

NDC Code 51079-482-20
Proprietary Name Venlafaxine Hydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-482-20) > 1 TABLET in 1 BLISTER PACK (51079-482-01)
Product NDC 51079-482
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name venlafaxine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120921
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
Substance Name VENLAFAXINE HYDROCHLORIDE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Venlafaxine Hydrochloride


General Information