# Omeprazole

NDC: 60505-3952
Generic name: Omeprazole
Labeler / Manufacturer: Apotex Corp
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20031111
Marketing ended: 20270131
FDA application: ANDA076048

## 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:"60505-3952"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60505-3952
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b83329ac-a65e-b3af-a3fb-c5a6c740e5e7