Glenmark Generics Inc., USA: 6 recalls on record

Recalls filed with 1 agency: FDA (6).

First recall on record: October 3, 2012. Most recent: April 16, 2014.

Risk classification: Class II: 2 · Class III: 4

Most recent recalls

DateAgencyProduct
April 16, 2014FDARanitidine Tablets USP, 150 mg, 500-count bottles, Rx only, Manufactured by: Shasun Pharm…D-1229-2014
May 22, 2013FDAGlenmark Gabapentin Tablets, a) 600mg, 500- count bottle (NDC 68462-126-05), b) 800 mg,…D-329-2013
May 22, 2013FDAGlenmark Pravastatin Sodium Tablets ,40 mg, 90-count bottle (NDC 68462-197-90), Rx only, …D-330-2013
May 22, 2013FDAGlenmark Topiramate Tablets, 200 mg, 60-count bottle, (NDC 68462-110-60), Rx only, Manuf…D-331-2013
March 13, 2013FDAMontelukast Sodium Tablets, 10 mg (base), packaged in a) 30-count tablets per bottle (NDC…D-182-2013
October 3, 2012FDANAPROXEN TABLETS USP, 500 mg, 100-count Tablets per bottle, Rx only, Manufactured by: Gle…D-1701-2012

Questions about this company

How many recalls does Glenmark Generics Inc., USA have?
Recalert has 6 U.S. recalls on record for Glenmark Generics Inc., USA, published between October 3, 2012 and April 16, 2014.
What was the most recent Glenmark Generics Inc., USA recall?
FDA recall D-1229-2014, published April 16, 2014: Ranitidine Tablets USP, 150 mg, 500-count bottles, Rx only, Manufactured by: Shasun Pharmaceuticals Limited, Unit-II R.S. No 32 33 & 34, Shasun Road, Periyakalapet, Puducherry, - 605 014, India; Manu…
Which agencies have handled Glenmark Generics Inc., USA recalls?
Glenmark Generics Inc., USA appears as the recalling firm in recalls from: FDA (6).

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