# Omeprazole

NDC: 63548-7370
Generic name: Omeprazole
Labeler / Manufacturer: PLD Acquisitions LLC DBA Avma Pharma Solutions
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20241031

FDA application: ANDA206582

## Active ingredients

- OMEPRAZOLE MAGNESIUM: 20.6 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63548-7370"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63548-7370
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=71add294-ff24-4bbf-9067-7c56ed7c9f1a