Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5825808 | Clinical Therapeutics | 2012 | 8 Pages |
Abstract
The test (dispersible) and reference tablets met the regulatory criteria for bioequivalence as defined by the SFDA. Both formulations were well tolerated. Chinese Clinical Trials registration number: ChiCTR-TRC-12001996.
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Authors
Mingzhu BPharma, Jianzhong PhD, Xingjiang MS, Junchun MS, Jian MS, Lihua MD,