Details for New Drug Application (NDA): 091272
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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 091272
Tradename: | VENLAFAXINE HYDROCHLORIDE |
Applicant: | Sun Pharm |
Ingredient: | venlafaxine hydrochloride |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Pharmacology for NDA: 091272
Mechanism of Action | Norepinephrine Uptake Inhibitors Serotonin Uptake Inhibitors |
Medical Subject Heading (MeSH) Categories for 091272
Suppliers and Packaging for NDA: 091272
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
VENLAFAXINE HYDROCHLORIDE | venlafaxine hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 091272 | ANDA | NorthStar RxLLC | 16714-038 | 16714-038-01 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-038-01) |
VENLAFAXINE HYDROCHLORIDE | venlafaxine hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 091272 | ANDA | NorthStar RxLLC | 16714-038 | 16714-038-02 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-038-02) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | EQ 37.5MG BASE | ||||
Approval Date: | Aug 18, 2010 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | EQ 75MG BASE | ||||
Approval Date: | Aug 18, 2010 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | EQ 150MG BASE | ||||
Approval Date: | Aug 18, 2010 | TE: | AB | RLD: | No |
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