Home DailyMed 679e53fe-9c99-442d-b6ff-4b3628ef4d16 OMEPRAZOLE MAGNESIUM DELAYED-RELEASE TABLETS Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer P & L Development, LLC
Effective date 2023-11-17
Label type HUMAN OTC DRUG LABEL
Version 1
Source full-release
Hydrated at 2026-06-01 00:32:15 Label at a glance# Product Omeprazole
Active ingredient OMEPRAZOLE MAGNESIUM
Label structure 16 sections
Dosage and administration for adults 18 years of age and older this product is to be used once a day (every 24 hours), every day for 14 days it may take 1 to 4 days for full effect; some people get complete relief of symptoms within 24 hours 14-Day Course of Treatment swallow 1 tablet with a glass of water before eating in the morning take everyday for 14 days do not take more than 1 tablet a day do not use for more than 14 days unless dir...
DailyMed RxNorm Mappings# RxCUI, RxNorm string, TTY table RxCUI RxNorm string TTY SPL version 402014 omeprazole 20 MG Delayed Release Oral Tablet PSN 1 402014 omeprazole 20 MG Delayed Release Oral Tablet SCD 1 402014 omeprazole 20 MG (as omeprazole magnesium 20.6 MG) Delayed Release Oral Tablet SY 1
DailyMed Pharmacologic Classes# DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59726-408-14 Omeprazole 1 in 1 BLISTER PACK TABLET, DELAYED RELEASE 1 1 59726-408-14 Omeprazole 14 in 1 CARTON TABLET, DELAYED RELEASE 14 1 59726-408-28 Omeprazole 1 in 1 BLISTER PACK TABLET, DELAYED RELEASE 1 1 59726-408-28 Omeprazole 28 in 1 CARTON TABLET, DELAYED RELEASE 28 1 59726-408-42 Omeprazole 1 in 1 BLISTER PACK TABLET, DELAYED RELEASE 1 1 59726-408-42 Omeprazole 42 in 1 CARTON TABLET, DELAYED RELEASE 42 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59726-408 OMEPRAZOLE TABLET, DELAYED RELEASE [P & L DEVELOPMENT, LLC] 1 6 package rows 20241101_679e53fe-9c99-442d-b6ff-4b3628ef4d16.zip
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 24 matching rows.
Omeprazole OMEPRAZOLE MAGNESIUM ACETYLTRIBUTYL CITRATE SILICON DIOXIDE STARCH, CORN CROSCARMELLOSE SODIUM DEXTROSE FD&C BLUE NO. 2 FD&C RED NO. 40 HYDROXYPROPYL CELLULOSE, UNSPECIFIED HYPROMELLOSE 2910 (15 MPA.S) MAGNESIUM STEARATE METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER POLYETHYLENE GLYCOL 400 POLYETHYLENE GLYCOL 3350 POLYETHYLENE GLYCOL 8000 POLYVINYL ALCOHOL, UNSPECIFIED PROPYLENE GLYCOL SUCROSE TALC TITANIUM DIOXIDE TRIACETIN TRIETHYL CITRATE MICROCRYSTALLINE CELLULOSE Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 23 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.