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ANI Pharmaceuticals Announces the FDA Approval and Launch of Trimethoprim Tablets USP

By AP News - Nov 16, 2022, 06:58 AM ET
Last Updated - Mar 27, 2024, 03:52 PM EDT
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ANI’s Trimethoprim Tablets are the generic version of the Reference Listed Drug (RLD) of the same established name. The current annual U.S. market for Trimethoprim Tablets is approximately $16.8 million, according to IQVIA/IMS Health, a leading healthcare data and analytics provider

ANI Pharmaceuticals, Inc. (ANI or the Company) (Nasdaq: ANIP) today announced that it received U.S. Food and Drug Administration (FDA) approval for the Abbreviated New Drug Application (ANDA) for Trimethoprim Tablets USP, 100 mg

BAUDETTE, Minn.--(BUSINESS WIRE)--Nov 16, 2022--

ANI Pharmaceuticals, Inc. (ANI or the Company) (Nasdaq: ANIP) today announced that it received U.S. Food and Drug Administration (FDA) approval for the Abbreviated New Drug Application (ANDA) for Trimethoprim Tablets USP, 100 mg.

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ANI’s Trimethoprim Tablets are the generic version of the Reference Listed Drug (RLD) of the same established name. The current annual U.S. market for Trimethoprim Tablets is approximately $16.8 million, according to IQVIA/IMS Health, a leading healthcare data and analytics provider.

"As we continue to focus on bringing niche limited-competition products to market, we are pleased to announce the FDA approval and commercialization of Trimethoprim Tablets,” stated Nikhil Lalwani, President and Chief Executive Officer of ANI.

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