Details for New Drug Application (NDA): 078517
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The generic ingredient in VENLAFAXINE HYDROCHLORIDE is venlafaxine hydrochloride. There are seventy-one drug master file entries for this compound. Sixty-eight suppliers are listed for this compound. Additional details are available on the venlafaxine hydrochloride profile page.
Summary for 078517
Tradename: | VENLAFAXINE HYDROCHLORIDE |
Applicant: | Pliva Hrvatska Doo |
Ingredient: | venlafaxine hydrochloride |
Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 078517
Profile for product number 001
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | EQ 25MG BASE | ||||
Approval Date: | Jun 13, 2008 | TE: | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | EQ 37.5MG BASE | ||||
Approval Date: | Jun 13, 2008 | TE: | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | EQ 50MG BASE | ||||
Approval Date: | Jun 13, 2008 | TE: | RLD: | No |
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