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Class II

Carvedilol Tablets, USP 12.5 mg, 500-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, India, Manufactured for: Glenmark Pharmaceuticals Inc. USA, Mahwah, NJ 07430 NDC# 68462-164-05.

CGMP Deviations

Recall number
D-0336-2025
Report date
April 16, 2025
Classification
Class II
Status in dataset
Ongoing
Recalling firm
Glenmark Pharmaceuticals Inc., USA
Generic names
CARVEDILOL
Brand names
CARVEDILOL
Product NDCs
68462-162, 68462-163, 68462-164, 68462-165

Code and lot information

Lot # 17240238, exp. date Jan-26 17240243, exp. date Jan-26 17240245, exp. date Jan-26 17240248, exp. date Jan-26

Distribution

U.S. Nationwide

Do not stop or change a prescribed medication based only on this page.Contact your pharmacist or prescriber and compare the exact product, manufacturer, NDC, and lot information.

Source and limitations

This page reflects a public openFDA Drug Enforcement record. The dataset was last checked on September 23, 2026. openFDA states that enforcement data should not be used alone to issue public alerts or track the full lifecycle of a recall.

Review the official FDA Drug Recalls page and the underlying openFDA query.