Elite Pharmaceuticals Receives FDA Approval for Generic Requip XL

Reuters
11/12
Elite Pharmaceuticals Receives FDA Approval for Generic Requip XL

Elite Pharmaceuticals Inc. announced that it has received approval from the US Food and Drug Administration (FDA) for its Abbreviated New Drug Application (ANDA) for a generic version of Requip XL® (Ropinirole Extended-Release Tablets USP) in 2 mg, 4 mg, 6 mg, 8 mg, and 12 mg strengths. The product, intended for the treatment of Parkinson's disease symptoms, will be marketed under the Elite Laboratories, Inc. label. According to IQVIA, the branded product and its equivalents recorded US sales of $10 million for the twelve months ending September 2025. The approval is exclusive to Elite Pharmaceuticals Inc.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Elite Pharmaceuticals Inc. published the original content used to generate this news brief via Newsfile (Ref. ID: 273940) on November 12, 2025, and is solely responsible for the information contained therein.

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