NDC 62332-234

VILAZODONE HYDROCHLORIDE

Vilazodone Hydrochloride

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

Product ID62332-234_268831b0-20c2-4999-a839-1ce5f428318d
NDC62332-234
Product TypeHuman Prescription Drug
Proprietary NameVILAZODONE HYDROCHLORIDE
Generic NameVilazodone Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2022-06-04
Marketing CategoryANDA /
Application NumberANDA208202
Labeler NameAlembic Pharmaceuticals Inc.
Substance NameVILAZODONE HYDROCHLORIDE
Active Ingredient Strength40 mg/1
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 62332-234-30

30 TABLET, FILM COATED in 1 BOTTLE (62332-234-30)
Marketing Start Date2022-06-04
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.