# Omeprazole

NDC: 51660-029
Generic name: Omeprazole
Labeler / Manufacturer: OHM LABORATORIES INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20190601

FDA application: ANDA207891

## Active ingredients

- OMEPRAZOLE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51660-029"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-029
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=35a95bec-51b9-465b-aa93-ad26afb87be8