US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 1, 2013 (13 years ago)

Nifedipine, extended-release tablets, 90mg 100 count blister pack, Rx only, Distributed…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Labeling: Incorrect or Missing Lot and/or Exp Date: Greenstone LLC is recalling Nifedipine Extended Release tablets (90mg). The expiration date on the package is 48 months instead of 36 months.

What was recalled

Nifedipine, extended-release tablets, 90mg 100 count blister pack, Rx only, Distributed by: GREENSTONE LLC, Pespack, NJ,07977, NDC 59762-6692-8

Recalling firm
Greenstone Llc
NDC code
59762-6692-8
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-737-2014

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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