# Rabeprazole Sodium

NDC: 62175-302
Generic name: Rabeprazole Sodium
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20131108

FDA application: ANDA090678

## Active ingredients

- RABEPRAZOLE SODIUM: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62175-302"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62175-302
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7f7d68f0-972b-4315-b712-0bb8a84c85cc