Zolmitriptan

NDC 46708-462 · Alembic Pharmaceuticals Limited

Generic nameZolmitriptan

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)ZOLMITRIPTAN

Strength2.5 mg/1

Pharmacologic classSerotonin 1b Receptor Agonists [MoA], Serotonin 1d Receptor Agonists [MoA], Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

Marketing categoryANDA

Packages

46708-462-06 — 6 TABLET, FILM COATED in 1 CARTON (46708-462-06)

FDA lists these products with the same active ingredient.

16571-803 — Zolmitriptan, 16571-804 — Zolmitriptan, 27241-021 — Zolmitriptan, 27241-022 — Zolmitriptan, 42291-998 — Zolmitriptan, 42291-999 — Zolmitriptan, 45802-711 — zolmitriptan, 46708-181 — Zolmitriptan, 46708-182 — Zolmitriptan, 46708-463 — Zolmitriptan, 59746-461 — Zolmitriptan, 59746-462 — Zolmitriptan, 60846-130 — zolmitriptan, 60846-133 — zolmitriptan, 62332-181 — Zolmitriptan, 62332-182 — Zolmitriptan, 62332-462 — Zolmitriptan, 62332-463 — Zolmitriptan, 63548-0101 — Zolmitriptan, 63548-0102 — Zolmitriptan, +25 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.