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VILAZODONE HYDROCHLORIDE

NDC 46708-233 · Alembic Pharmaceuticals Limited

Generic nameVILAZODONE HYDROCHLORIDE
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)VILAZODONE HYDROCHLORIDE
Strength20 mg/1
Marketing categoryANDA

Packages

46708-233-30 — 30 TABLET, FILM COATED in 1 BOTTLE (46708-233-30)

46708-233-71 — 500 TABLET, FILM COATED in 1 BOTTLE (46708-233-71)

46708-233-90 — 90 TABLET, FILM COATED in 1 BOTTLE (46708-233-90)

46708-233-91 — 1000 TABLET, FILM COATED in 1 BOTTLE (46708-233-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0456-1110 — vilazodone hydrochloride, 0456-1120 — vilazodone hydrochloride, 0456-1140 — vilazodone hydrochloride, 0480-2043 — Vilazodone Hydrochloride, 0480-2044 — Vilazodone Hydrochloride, 0480-2045 — Vilazodone Hydrochloride, 16729-352 — Vilazodone Hydrochloride, 16729-353 — Vilazodone Hydrochloride, 16729-354 — Vilazodone Hydrochloride, 46708-232 — VILAZODONE HYDROCHLORIDE, 46708-234 — VILAZODONE HYDROCHLORIDE, 51407-915 — Vilazodone Hydrochloride, 51407-916 — Vilazodone Hydrochloride, 51407-917 — Vilazodone Hydrochloride, 60505-4372 — vilazodone hydrochloride, 60505-4373 — vilazodone hydrochloride, 60505-4374 — vilazodone hydrochloride, 62332-232 — VILAZODONE HYDROCHLORIDE, 62332-233 — VILAZODONE HYDROCHLORIDE, 62332-234 — VILAZODONE HYDROCHLORIDE, +15 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.