News
27 Oct 2011
FDA Nods for Sagent Bupivacaine Hydrochloride Injection
Sagent Pharmaceuticals' bupivacaine hydrochloride injection wins FDA approval and will be available in six single-dose and two multi-dose latex-free vials.
The US FDA has granted approval for US-based Sagent Pharmaceuticals' bupivacaine hydrochloride injection.
The drug is indicated for the production of local or regional anaesthesia or analgaesia for dental and oral surgery procedures, diagnostic and therapeutic procedures, and obstetrical procedures.
Developed by Strides Arcolab, the injection will be available in six single-dose and two multi-dose latex-free vials.
Strides is responsible for developing and supplying injectable products that Sagent will market in the US.
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