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MMWR: Food and Drug Administration Approval for Use of Hiberix as a 3-Dose Primary Haemophilus influ

Thursday, April 28, 2016   (0 Comments)

On January 14, 2016, GlaxoSmithKline Biologicals (Research Triangle Park, North Carolina) received approval from the Food and Drug Administration (FDA) to expand use of Hiberix (Haemophilus b Conjugate Vaccine [Tetanus Toxoid Conjugate]) for a 3-dose infant primary vaccination series at ages 2, 4, and 6 months.

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