NDC 76282-544

Vilazodone Hydrochloride

Vilazodone Hydrochloride

Vilazodone Hydrochloride is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Exelan Pharmaceuticals Inc.. The primary component is Vilazodone Hydrochloride.

Product ID76282-544_abfc9ce0-a387-4f42-98a8-41a619946412
NDC76282-544
Product TypeHuman Prescription Drug
Proprietary NameVilazodone Hydrochloride
Generic NameVilazodone Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2022-12-01
Marketing CategoryANDA /
Application NumberANDA208200
Labeler NameExelan Pharmaceuticals Inc.
Substance NameVILAZODONE HYDROCHLORIDE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 76282-544-30

30 TABLET, FILM COATED in 1 BOTTLE (76282-544-30)
Marketing Start Date2022-12-01
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Vilazodone Hydrochloride" or generic name "Vilazodone Hydrochloride"

NDCBrand NameGeneric Name
0480-2043Vilazodone HydrochlorideVilazodone Hydrochloride
0480-2044Vilazodone HydrochlorideVilazodone Hydrochloride
0480-2045Vilazodone HydrochlorideVilazodone Hydrochloride
16729-352Vilazodone HydrochlorideVilazodone Hydrochloride
16729-353Vilazodone HydrochlorideVilazodone Hydrochloride
16729-354Vilazodone HydrochlorideVilazodone Hydrochloride
0456-1100VIIBRYDvilazodone hydrochloride
0456-1101VIIBRYDvilazodone hydrochloride
0456-1110VIIBRYDvilazodone hydrochloride
0456-1120VIIBRYDvilazodone hydrochloride
0456-1140VIIBRYDvilazodone hydrochloride
55154-4624VIIBRYDvilazodone hydrochloride
55154-4627VIIBRYDvilazodone hydrochloride
51407-691vilazodonevilazodone hydrochloride
51407-692Vilazodonevilazodone hydrochloride
51407-693Vilazodonevilazodone hydrochloride

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.