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venlafaxine hydrochloride - 68382-034-16 - (venlafaxine hydrochloride)

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Drug Information of venlafaxine hydrochloride

Product NDC: 68382-034
Proprietary Name: venlafaxine hydrochloride
Non Proprietary Name: venlafaxine hydrochloride
Active Ingredient(s): 37.5    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: 68382-034
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090174
Marketing Category: ANDA
Start Marketing Date: 20110601

Package Information of venlafaxine hydrochloride

Package NDC: 68382-034-16
Package Description: 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-034-16)

NDC Information of venlafaxine hydrochloride

NDC Code 68382-034-16
Proprietary Name venlafaxine hydrochloride
Package Description 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-034-16)
Product NDC 68382-034
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name venlafaxine hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110601
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) Inc.
Substance Name VENLAFAXINE HYDROCHLORIDE
Strength Number 37.5
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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