# Omeprazole

NDC: 63187-170
Generic name: Omeprazole
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20090121
Marketing ended: 20270131
FDA application: ANDA076048

## Active ingredients

- OMEPRAZOLE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63187-170"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63187-170
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=253451a6-02a9-4b27-aed7-f3dbc2e09682