Reported Jul 17, 2013 · Terminated

Nimodipine Capsules 30 mg, Rx Only, For Institutional Use Only, a) 30-count unit dose Capsules (5x6 blister cards per…

Sun Pharmaceutical Industries Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Sun Pharmaceutical Industries Inc. · 270 Prospect Plains Rd · Cranbury, NJ · 08512-3605

Is this the product you have?

  • Nimodipine Capsules 30 mg, Rx Only, For Institutional Use Only, a) 30-count unit dose Capsules (5x6 blister cards per carton), NDC 57664-135-64, b) 100-count unit dose Capsules (25x4 blister cards per carton), NDC 57664-135-65
  • Distributed byCaraco Pharmaceutical Laboratories, Ltd. Detroit, MI 48202 Affiliate of Sun Pharmaceutical Industries, Inc
Lot codes and dates
    • Lot #s: a) 3305.036B
    • 3305.037B
    • Exp Jun-13
    • 3505.041B
    • Exp Sep-13
    • 3305.043B
    • Exp Nov-13
    • 3305.044B
    • Exp Dec-13
    • 3305.045B Mar-14. Lot #s: b) 3305.036A
    • 3305.037A
    • Exp Jun-13
    • 3305.038A
    • Exp Jul-13
    • 3305.040A
    • 3505.041A Exp Sep-13
    • 3305.042A
    • 3305.043A
    • Exp Nov-13
    • 3305.044A Dec-13
Amount recalled
46387 Cartons

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Crystallization; crystallized nimodipine

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Aug 25, 2014 · Data as of Sep 19, 7:21 PM UTC

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