Generic omeprazole delayed-release capsules: in vitro performance evaluations

Terry Moore Office of Testing and Research, Division of Pharmaceutical Analysis, Food and Drug Administration, St. Louis, MO, USACorrespondence[email protected]

Anjanette Smith Office of Testing and Research, Division of Pharmaceutical Analysis, Food and Drug Administration, St. Louis, MO, USA

Wei Ye Office of Testing and Research, Division of Pharmaceutical Analysis, Food and Drug Administration, St. Louis, MO, USA

Duckhee Y. Toler Office of Testing and Research, Division of Pharmaceutical Analysis, Food and Drug Administration, St. Louis, MO, USA

Benjamin J. Westenberger Office of Testing and Research, Division of Pharmaceutical Analysis, Food and Drug Administration, St. Louis, MO, USA

Robert Lionberger Office of Generic Drugs, Food and Drug Administration, Rockville, MD, USA

Andre Raw Office of Generic Drugs, Food and Drug Administration, Rockville, MD, USA

Lawrence Yu Office of Generic Drugs, Food and Drug Administration, Rockville, MD, USA

Lucinda F. Buhse Office of Testing and Research, Division of Pharmaceutical Analysis, Food and Drug Administration, St. Louis, MO, USA

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References

Farinha A, Bica A, Martins JM, Pais JP. (2000). Dissolution of omeprazole from delayed-release solid oral dosage forms. Drug Dev Ind Pharm., 26:785–90.
PubMed Web of Science ®Google Scholar
Robb-Nicholson C. (2007). By the way, doctor: Are generic and brand-name drugs really the same? Harv Womens Health Watch, 14(5):8.
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Udd M, Toyry J, Miettinen P, Vanninen E, Mustonen H, Julkunen R. (2005). The effect of regular and high doses of omeprazole on the intragastric acidity in patients with bleeding peptic ulcer treated endoscopically: A clinical trial with continuous intragastic pH monitoring. Eur J Gastroenterol Hepatol, 17:1351–6.
PubMed Web of Science ®Google Scholar

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