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Purdue Pharma Has Obtained Approval From The US Food and Drug Administration
Sep 27, 2013Purdue Pharma has obtained approval from the US Food and Drug Administration (FDA) for the launch of a new 15mcg/hr dosage strength of Butrans (buprenorphine) Transdermal System CIII. Following the approval, Butrans will be available in ...
Tags: Pain Drug, Purdue Pharma
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Upsher-Smith Will Launch The Generic Version of Its Morphine Sulfate ER Capsules
Sep 3, 2013US-based specialty pharmaceutical firm Upsher-Smith Laboratories will launch the generic version of its Morphine Sulfate extended-release (ER) capsules, CII on 4 September 2013. Morphine Sulfate ER Capsules, CII are currently available in ...
Tags: ER Capsules, pharmaceutical
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Upgrade Allows Improves Performance of Printheads and Is Available in Reel-to-Reel
Mar 11, 2013The upgrade allows improves the performance of the printheads and is available in reel-to-reel or inline formats. The product targets the pharmaceutical sector and the system offers full digital four-colour print. “Variations in ...
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Novartis Obtained FDA Approval for a New 13.3 Mg/24 H Dosage Strength of Its Exelon Patch
Dec 5, 2012Novartis has obtained the US Food and Drug Administration (FDA) approval for a new 13.3 mg/24 h dosage strength of its Exelon Patch (rivastigmine transdermal system), designed to treat patients with mild to moderate Alzheimer's disease. ...
Tags: Alzheimer's disease, Novartis Pharmaceuticals, Exelon Patch
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Baxter Receives The US FDA Approval for Its 4000 Iu Dosage Strength of Advate
Jul 18, 2012Baxter International has received the US Food and Drug Administration (FDA) approval for its 4000 IU dosage strength of Advate[Antihemophilic Factor (Recombinant), Plasma/Albumin-Free Method]. Advate is a full-length recombinant factor ...
Tags: FDA, Baxter hemophilia drug, dosage strength
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