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VIIBRYD
VIIBRYD - 0456-1120-30 - (vilazodone hydrochloride)
Drug Information of VIIBRYD
| Product NDC: | 0456-1120 |
| Proprietary Name: | VIIBRYD |
| Non Proprietary Name: | vilazodone hydrochloride |
| Active Ingredient(s): | 20 mg/1 & nbsp; vilazodone hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of VIIBRYD
| Product NDC: | 0456-1120 |
| Labeler Name: | Forest Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022567 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110429 |
Package Information of VIIBRYD
| Package NDC: | 0456-1120-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (0456-1120-30) |
NDC Information of VIIBRYD
| NDC Code | 0456-1120-30 |
| Proprietary Name | VIIBRYD |
| Package Description | 30 TABLET in 1 BOTTLE (0456-1120-30) |
| Product NDC | 0456-1120 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | vilazodone hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110429 |
| Marketing Category Name | NDA |
| Labeler Name | Forest Laboratories, Inc. |
| Substance Name | VILAZODONE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
