# pantoprazole sodium

NDC: 70010-191
Generic name: pantoprazole sodium
Labeler / Manufacturer: Granules Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20240412

FDA application: ANDA217282

## Active ingredients

- PANTOPRAZOLE SODIUM: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70010-191"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70010-191
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8f2fb647-15bc-41cb-84a4-02e956e614fc