United States · FDA National Drug Code directory

zolmiptriptan

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
68462-499_977ca814-2c55-4de0-a75e-9e42f2e86f77
Product NDC
68462-499
Form
TABLET, ORALLY DISINTEGRATING
Composition / generic term
zolmitriptan
Labeler
Glenmark Pharmaceuticals Inc., USA
Marketing category
ANDA
Marketing start / end (source format)
20130514
Source listing expiry
20271231

Source-listed ingredients

  • ZOLMITRIPTAN — 2.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BLISTER PACK in 1 CARTON (68462-499-76) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (68462-499-40) · 68462-499-76

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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zolmiptriptan — United States | Molindra Medicines