Drug & medication recalls Moderate risk

Frovatriptan Succinate Tablets 2 recalled over manufacturing violations

Recall date
March 13, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
Glenmark Pharmaceuticals Inc., USA recalls Frovatriptan Succinate Tablets 2.5mg, 9-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pitha…
Recall number
D-0322-2025
FDA classification
Class II
Brand / firm
Glenmark Pharmaceuticals Inc., USA
Sold / distributed
U.S. Nationwide

Why it was recalled

CGMP Deviations

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Frovatriptan Succinate Tablets 2.5mg, 9-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, India, Manufactured for: Glenmark Pharmaceuticals Inc. USA, Mahwah, NJ 07430. NDC# 68462-694-97

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