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Zydus secures USFDA approval for Gabapentin tablets - The Hindu BusinessLine

Zydus secures USFDA approval for Gabapentin tablets - The Hindu BusinessLine
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United States , Drug Administration , Zydus Lifesciences , Zydus Lifesciences Limited , United States Food , Gabapentin Tablets , Postherpetic Neuralgia , Propranolol Hydrochloride , Abbreviated New Drug Applications ,

Zydus gets USFDA nod for generic medication

Zydus Lifesciences announced that it has obtained approval from the USFDA to sell a generic medication for the treatment of postherpetic neuralgia. The company has received the final nod from the US Food and Drug Administration (USFDA) to produce and distribute Gabapentin tablets in strengths of 300 mg and 600 mg, as stated in a regulatory filing by Zydus Lifesciences. ....

New Delhi , Zydus Lifesciences , Drug Administration , Generic Medication , Gabapentin Tablets , Postherpetic Neuralgia ,

Zydus Receives USFDA Approval for Generic Medication | India News

India News: Zydus Lifesciences has received approval from the US Food and Drug Administration (USFDA) to market a generic medication to manage postherpetic neuralgia. Read more. ....

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Granules India : Gabapentin Tabs Approval – Press Release

Press Release

For Immediate Release

Granules India Limited Received ANDA Approval for

Gabapentin Tablets

. | March 29, 2023 ....

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Zydus receives tentative approval from the USFDA for Gabapentin tablets

Zydus Lifesciences Limited’s subsidiary, Zydus Pharmaceuticals (USA) Inc., has received tentative approval from the United States Food and Drug Administration (USFDA) for Gabapentin Tablets, the company said via an exchange filing.

The recommended daily dose is 300 mg or 600 mg (Gralise Tablets).

Gabapentin tablets are indicated for the management of Postherpetic Neuralgia (PHN). ....

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