Pantoprazole Sodium 40 mg DR Tablets Under Non-Fasting Conditions

Criteria for Evaluation: FDA Bioequivalence Criteria

Statistical Methods: FDA bioequivalence statistical methods

Inclusion Criteria:

- All subjects selected for this study will be non-smokers at least 18 years of age.
Subjects will have a BMI (Body Mass Index) of 30 or less.

Exclusion Criteria:

- Subjects with a significant recent history of chronic alcohol consumption (past 2
years), drug addiction, or serious gastrointestinal, renal, hepatic or cardiovascular,
disease, tuberculosis, epilepsy, asthma (past 5 years), diabetes, psychosis or
glaucoma will not be eligible for this study.

- Subjects whose clinical laboratory test values are greater than 20% outside the normal
range may be retested. If the clinical values are outside the range on retesting, the
subject will not be eligible to participate in the study unless the clinical
investigator deems the result not to be significant.

- Subjects who have a history of allergic responses to the class of drug being tested
will be excluded from the study.

- All subjects will have urine samples assayed for the presence of drugs of abuse as
part of the clinical laboratory screening procedures and at each dosing period
check-in. Subjects found to have urine concentrations of any of the tested drugs will
not be allowed to participate.

- Subjects should not have donated blood and/ot plasma for at least thirty (30) days
prior to the first dosing of the study.

- Subjects who have taken any investigational drug within thirty (30) days prior to the
first dosing of the study will not be allowed to participate.

- Female subjects who are pregnant, breast-feeding, or who are likely to become pregnant
during the study will not be allowed to participate. Female subjects of child bearing
potential must either abstain from sexual intercourse or use a reliable barrier method
(e.g. condom, IUD) of contraception during the course of the study (first dosing until
last blood collection) or they will not be allowed to participate. Subjects who have
used implanted or injected hormonal contraceptives anytime during the 180 days prior
to study dosing or oral hormonal contraceptives with in 14 days of dosing will not be
allowed to participate.

- All female subjects will be screened for pregnancy at check-in each study period.
Subjects with positive or inconclusive results will be with drawn from the study.

- Subjects who do not tolerate venipuncture will not be allowed to participate.

- Subjects who use tobacco in any form will not be eligible to participate in the study.
Three months abstinence is required.