Details for New Drug Application (NDA): 090899
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The generic ingredient in VENLAFAXINE HYDROCHLORIDE is venlafaxine hydrochloride. There are seventy-one drug master file entries for this compound. Seventy suppliers are listed for this compound. Additional details are available on the venlafaxine hydrochloride profile page.
Summary for 090899
Tradename: | VENLAFAXINE HYDROCHLORIDE |
Applicant: | Torrent |
Ingredient: | venlafaxine hydrochloride |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Pharmacology for NDA: 090899
Mechanism of Action | Norepinephrine Uptake Inhibitors Serotonin Uptake Inhibitors |
Medical Subject Heading (MeSH) Categories for 090899
Suppliers and Packaging for NDA: 090899
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
VENLAFAXINE HYDROCHLORIDE | venlafaxine hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 090899 | ANDA | Major Pharmaceuticals | 0904-6468 | 0904-6468-61 | 100 BLISTER PACK in 1 CARTON (0904-6468-61) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK |
VENLAFAXINE HYDROCHLORIDE | venlafaxine hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 090899 | ANDA | Major Pharmaceuticals | 0904-6469 | 0904-6469-61 | 100 BLISTER PACK in 1 CARTON (0904-6469-61) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK |
Profile for product number 001
Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | EQ 37.5MG BASE | ||||
Approval Date: | Jun 1, 2011 | TE: | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | EQ 75MG BASE | ||||
Approval Date: | Jun 1, 2011 | TE: | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | EQ 150MG BASE | ||||
Approval Date: | Jun 1, 2011 | TE: | RLD: | No |
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