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Venlafaxine hydrochloride - 64455-107-90 - (Venlafaxine hydrochloride)

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Drug Information of Venlafaxine hydrochloride

Product NDC: 64455-107
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): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Venlafaxine hydrochloride

Product NDC: 64455-107
Labeler Name: BTA Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090071
Marketing Category: ANDA
Start Marketing Date: 20130101

Package Information of Venlafaxine hydrochloride

Package NDC: 64455-107-90
Package Description: 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (64455-107-90)

NDC Information of Venlafaxine hydrochloride

NDC Code 64455-107-90
Proprietary Name Venlafaxine hydrochloride
Package Description 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (64455-107-90)
Product NDC 64455-107
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Venlafaxine hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130101
Marketing Category Name ANDA
Labeler Name BTA Pharmaceuticals
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


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