Details for New Drug Application (NDA): 208212
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The generic ingredient in VILAZODONE HYDROCHLORIDE is vilazodone hydrochloride. There are fourteen drug master file entries for this compound. Fourteen 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 |
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