# Omeprazole delayed release

NDC: 49483-731
Generic name: Omeprazole 20mg
Labeler / Manufacturer: TIME CAP LABORATORIES, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20251215

FDA application: ANDA218829

## Active ingredients

- OMEPRAZOLE MAGNESIUM: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"49483-731"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49483-731
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=40906798-cd84-fbd0-e063-6294a90a1d29