Zydus Lifesciences arm gets USFDA nod for Postherpetic Neuralgia drug Gabapentin
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Ahmedabad: Pharma major Zydus Lifesciences Limited has announced that the company's subsidiary Zydus Pharmaceuticals (USA) Inc. has received tentative approval from the United States Food and Drug Administration (USFDA) for Gabapentin Tablets (Once-Daily), 300 mg and 600 mg (USRLD: Gralise Tablets).
Gabapentin tablets are indicated for the management of Postherpetic Neuralgia (PHN). Postherpetic neuralgia is neuropathic pain that occurs due to damage to a peripheral nerve caused by the reactivation of the varicella zoster virus.
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