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ADMA Biologics receives FDA approval for license transfers for BIVIGAM® and Nabi-HB®
ADMA Biologics announces the FDA has notified ADMA the licenses for BIVIGAM® and Nabi-HB® have been revoked from Biotest Pharmaceuticals, U.S. License No. 1792 and transferred and issued to ADMA’s U.S. License No. 2019.
July 08, 2019
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