FULL PRESCRIBING INFORMATION 1 INDICATIONS AND USAGE PROTONIX For Delayed-Release Oral Suspension and PROTONIX Delayed-Release Tablets are indicated for: 1
• PROTONIX for oral
4 to 13
0 For information on how to adjust dosing for individual patient needs, see the full prescribing information
• For information on how to prepare and administer for each indication, see the full Fifteen Minute Infusion
Maximum dose: 240 mg/day
Administration (2
(intravenous pantoprazole sodium) for Injection is a substituted benzimidazole, sodium 5-(difluoromethoxy)-2-[[(3,4-dimethoxy-2-pyridinyl)methyl] sulfinyl]-1H-benzimidazole, a
Pantoprazole is in a class of medications called proton-pump inhibitors
3
For non-prescription products, read the label or package ingredients carefully
4 to 13
Children 5 years of age and older weighing 40 kilograms (kg) or more—40 mg once a day for up to 8 weeks
Pantoprazole Sodium for Injection is supplied for intravenous administration as a sterile lyophilized powder in a single-dose clear glass vial fitted with a rubber stopper and crimp seal
Tell your doctor if you have lupus
Following the initial oral dose of 40 mg
Pantoprazole injection is used to treat certain conditions in which there is too much acid in the stomach
is supplied for intravenous administration as a sterile, freeze-dried powder in a single-dose clear glass vial fitted with a rubber stopper and crimp seal
(pantoprazole sodium), a PPI, is a substituted benzimidazole, sodium 5-(difluoromethoxy)-2-[[(3,4-dimethoxy-2-pyridinyl)methyl] sulfinyl] 1H-benzimidazole, a compound that inhibits gastric acid secretion
(pantoprazole sodium) is supplied in a single-dose vial as a white to off-white freeze-dried powder for reconstitution containing 40 mg of pantoprazole