Evaluation of Pharmacokinetics and Safety with Bioequivalence of Ibuprofen Sustained-Release Capsules of Two Formulations, in Chinese Healthy Volunteers: Bioequivalence Study-Reference-Cited by-同舟云学术

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Evaluation of Pharmacokinetics and Safety with Bioequivalence of Ibuprofen Sustained-Release Capsules of Two Formulations, in Chinese Healthy Volunteers: Bioequivalence Study

Published:2023-06 Issue: Volume:Volume 17 Page:1881-1888
ISSN:1177-8881
Container-title:Drug Design, Development and Therapy
language:en
Short-container-title:DDDT

Author:

Huang Chunqi,Yin Zhou,Yang Yeqing,Mo Nan,Yang Hui,Wang Ying^ORCID

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmaceutical Science,Pharmacology

Reference19 articles.

1. Pharmacokinetics, Bioequivalence, and Safety Evaluation of Two Formulations of 0.2‐g Ibuprofen Granules

2. Chiral bioanalytical methods in bioequivalence studies of intravenous vs. oral formulations of ibuprofen

3. Bioequivalence assessment of two formulations of ibuprofen

4. The pharmacokinetic profile of a novel fixed-dose combination tablet of ibuprofen and paracetamol

5. Nonsteroidal Anti-inflammatory Drugs Dampen the Cytokine and Antibody Response to SARS-CoV-2 Infection

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1. Pharmacokinetic, bioequivalence, and safety assessments of two brands of 30-mg nifedipine controlled-release formulations in Chinese healthy subjects;Int. Journal of Clinical Pharmacology and Therapeutics;2024-07-30

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