# Omeprazole

NDC: 68382-412
Generic name: Omeprazole
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20121123

FDA application: ANDA091352

## 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:"68382-412"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68382-412
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c22ceb2-2c34-43c3-9a35-2589c9078741