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Venlafaxine Hydrochloride - 21695-957-30 - (venlafaxine hydrochloride)

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Drug Information of Venlafaxine Hydrochloride

Product NDC: 21695-957
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: 21695-957
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020699
Marketing Category: NDA
Start Marketing Date: 20110610

Package Information of Venlafaxine Hydrochloride

Package NDC: 21695-957-30
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (21695-957-30)

NDC Information of Venlafaxine Hydrochloride

NDC Code 21695-957-30
Proprietary Name Venlafaxine Hydrochloride
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (21695-957-30)
Product NDC 21695-957
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name venlafaxine hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110610
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
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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