Granules India receives USFDA approval for Methocarbamol Tablet

08 May 2018 Evaluate

Granules India has received an approval from the US Food & Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) filed by it for Methocarbamol Tablet 500 mg and 750 mg. The approved ANDA is the bioequivalent and therapeutically equivalent to Reference Listed Drug (RLD) of Robaxin 500 mg and 750 mg of Auxilium Pharmaceuticals. LLC. The company intends to commercialize this product shortly.

Granules India is manufacturer and supplier of pharmaceutical products. Its products include active pharmaceutical ingredients (API) like tablets, caplets, rapid release, pharmaceutical, formulation intermediates (PFI) and Finished Dosages (FDs).

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564.95 -6.25 (-1.09%)
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