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NDC 65862-0559-90

Pantoprazole Sodium 20 mg/1 TABLET, DELAYED RELEASE

Aurobindo Pharma Limited

In Stock at Premier Pharma
NDC
65862-0559-90
Generic Name
Pantoprazole Sodium
Brand Name
Pantoprazole Sodium
Strength
20 mg/1
Dosage Form
TABLET, DELAYED RELEASE
Route
ORAL
Package Size
—
Labeler
Aurobindo Pharma Limited

FDA Drug Information

Indications & Usage

1 INDICATIONS AND USAGE Pantoprazole sodium delayed-release tablets are indicated for: Pantoprazole sodium is a proton pump inhibitor (PPI) indicated for the following: Short-Term Treatment of Erosive Esophagitis Associated with Gastroesophageal Reflux Disease (GERD) (1.1) Maintenance of Healing of Erosive Esophagitis (1.2) Pathological Hypersecretory Conditions Including Zollinger-Ellison (ZE) Syndrome (1.3) 1.1 Short-Term Treatment of Erosive Esophagitis Associated With Gastroesophageal Reflux…

Source: FDA. For professional use only. Not a substitute for prescribing information.

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Other Pantoprazole Sodium NDC Codes

65862-0560-9940MGTABLET, DELAYED RELEASE
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55150-0202-1040 mg/1INJECTION, POWDER, FOR SOLUTION
2-Day
62756-0129-4440 mg/10mLINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
2-Day

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