Details for New Drug Application (NDA): 090174
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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-two suppliers are listed for this compound. Additional details are available on the venlafaxine hydrochloride profile page.
Summary for 090174
| Tradename: | VENLAFAXINE HYDROCHLORIDE |
| Applicant: | Zydus Pharms Usa Inc |
| Ingredient: | venlafaxine hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 090174
| Mechanism of Action | Norepinephrine Uptake Inhibitors Serotonin Uptake Inhibitors |
Medical Subject Heading (MeSH) Categories for 090174
Suppliers and Packaging for NDA: 090174
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| VENLAFAXINE HYDROCHLORIDE | venlafaxine hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 090174 | ANDA | A-S Medication Solutions | 50090-6301 | 50090-6301-0 | 33 BLISTER PACK in 1 CARTON (50090-6301-0) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK |
| VENLAFAXINE HYDROCHLORIDE | venlafaxine hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 090174 | ANDA | Zydus Lifesciences Limited | 65841-751 | 65841-751-06 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-751-06) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | EQ 37.5MG BASE | ||||
| Approval Date: | Apr 14, 2011 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | EQ 75MG BASE | ||||
| Approval Date: | Apr 14, 2011 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | EQ 150MG BASE | ||||
| Approval Date: | Apr 14, 2011 | TE: | AB | RLD: | No | ||||
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