D-737-2014 Class II Terminated
FDA drug recall D-737-2014 was initiated by Greenstone Llc on November 1, 2013 and is designated Class II. Reason for recall: 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. The recall status is terminated (terminated June 5, 2015). Affected quantity: 21600 tablets.
Recall Details
- Product Type
- Drugs
- Report Date
- January 22, 2014
- Initiation Date
- November 1, 2013
- Termination Date
- June 5, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 21600 tablets
Product Description
Nifedipine, extended-release tablets, 90mg 100 count blister pack, Rx only, Distributed by: GREENSTONE LLC, Pespack, NJ,07977, NDC 59762-6692-8
Reason for Recall
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.
Distribution Pattern
Nationwide
Code Information
V110079