# Pantoprazole Sodium

NDC: 65162-636
Generic name: Pantoprazole
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20160620

FDA application: ANDA205119

## Active ingredients

- PANTOPRAZOLE SODIUM: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65162-636"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65162-636
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f3ded82a-cf0d-4844-944a-75f9f9215ff0