Details for New Drug Application (NDA): 208212
The generic ingredient in VILAZODONE HYDROCHLORIDE is vilazodone hydrochloride. There is one drug master file entry for this compound. Thirteen suppliers are listed for this compound. Additional details are available on the vilazodone hydrochloride profile page.
Summary for 208212
| Tradename: | VILAZODONE HYDROCHLORIDE |
| Applicant: | Teva Pharms Usa |
| Ingredient: | vilazodone hydrochloride |
| Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 208212
Suppliers and Packaging for NDA: 208212
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| VILAZODONE HYDROCHLORIDE | vilazodone hydrochloride | TABLET;ORAL | 208212 | ANDA | Teva Pharmaceuticals, Inc. | 0480-2043 | 0480-2043-56 | 30 TABLET, FILM COATED in 1 BOTTLE (0480-2043-56) |
| VILAZODONE HYDROCHLORIDE | vilazodone hydrochloride | TABLET;ORAL | 208212 | ANDA | Teva Pharmaceuticals, Inc. | 0480-2044 | 0480-2044-56 | 30 TABLET, FILM COATED in 1 BOTTLE (0480-2044-56) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
| Approval Date: | Sep 30, 2019 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 20MG | ||||
| Approval Date: | Sep 30, 2019 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 40MG | ||||
| Approval Date: | Sep 30, 2019 | TE: | AB | RLD: | No | ||||
Complete Access Available with Subscription
