# RABEPRAZOLE SODIUM

NDC: 72189-142
Generic name: RABEPRAZOLE SODIUM
Labeler / Manufacturer: DIRECT RX
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20201015

FDA application: ANDA205761

## 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:"72189-142"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-142
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b1b7def0-834f-37f5-e053-2a95a90ade1f