Biofrontera Announces FDA Has Approved Co.'s sNDA To Increase Maximally Approved Dosage From One To Three Tubes Of Ameluz Topical Gel Per Treatment
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Biofrontera has received FDA approval for its supplemental New Drug Application (sNDA) to increase the maximum approved dosage of Ameluz topical gel from one to three tubes per treatment. This approval could potentially enhance the product's marketability and sales.
October 07, 2024 | 12:46 pm
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Biofrontera's FDA approval for increasing the dosage of Ameluz gel from one to three tubes per treatment could lead to increased sales and market presence.
The FDA approval allows Biofrontera to market Ameluz gel with a higher dosage, which can lead to increased usage and sales. This regulatory milestone is significant for the company's growth prospects.
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