Indoco Remedies secures USFDA nod for Lofexidine Tablets 0.18 mg
Written By : Ruchika Sharma
Medically Reviewed By : Dr. Kamal Kant Kohli
Published On 2024-08-22 07:00 GMT | Update On 2024-08-22 07:01 GMT
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Mumbai: Indoco Remedies Limited has announced the receipt of final approval from the U.S. Food and Drug Administration (USFDA) for Abbreviated New Drug Application (ANDA) for Lofexidine Tablets 0.18 mg to market a generic equivalent of Lucemyra Tablets, 0.18 mg of USWM, LLC.
Indoco has been granted a Competitive Generic Therapy (CGT) designation by the USFDA and being the first approved generic, is eligible for 180 days of CGT exclusivity for Lofexidine Tablets, 0.18 mg (“Product”) in the USA. This exclusivity will begin to run from the date of the first commercial marketing of the product. Indoco intends to launch the product immediately in the USA.
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