Press Statement Issued by Ranbaxy Laboratories Limited
Posted on: Wednesday, 25 February 2009, 14:23 CST
GURGAON,
The FDA has said it has no evidence the drugs on the market are substandard and also that they comply with specifications upon testing.
No products from Ranbaxy's other manufacturing facilities are included in the AIP.
Ranbaxy will continue to co-operate with the USFDA. Further, no effort or action will be spared to timely protect key ANDAs from Paonta Sahib, which include some First to File applications.
Ranbaxy Laboratories Limited,
SOURCE Ranbaxy Laboratories Limited
Source: PR Newswire
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