FDA.reportPublic FDA data

NDC 43598-286-70 - Omeprazole

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
43598-286
Requested NDC
43598-286-70
Package NDCs from labels
43598-286-52, 43598-286-27, 43598-286-33, 43598-286-74, 43598-286-25, 43598-286-37, 43598-286-70, 43598-286-32
Manufacturer
Dr. Reddys Laboratories Inc | Dr.Reddy's Laboratories Limited (SEZ UNIT)
Effective date
2024-12-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Omeprazole Delayed Release TabletsDr. Reddys Laboratories Inc | Dr.Reddy's Laboratories Limited (SEZ UNIT)2024-12-19HUMAN OTC DRUG LABEL
Omeprazole - Walgreens CompanyWalgreens Company2024-11-10HUMAN OTC DRUG LABEL
Omeprazole Delayed Release TabletsThirty Madison Inc | Dr.Reddy's Laboratories Limited (SEZ UNIT) | Reed Lane Inc2024-10-28HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43598-286-25Omeprazole14 in 1 BLISTER PACKTABLET, DELAYED RELEASE147
43598-286-25Omeprazole2 in 1 CARTONTABLET, DELAYED RELEASE27
43598-286-27Omeprazole2 in 1 CARTONTABLET, DELAYED RELEASE27
43598-286-32Omeprazole2 in 1 CARTONTABLET, DELAYED RELEASE27
43598-286-33Omeprazole3 in 1 CARTONTABLET, DELAYED RELEASE37
43598-286-37Omeprazole3 in 1 CARTONTABLET, DELAYED RELEASE37
43598-286-37Omeprazole14 in 1 BLISTER PACKTABLET, DELAYED RELEASE147
43598-286-52Omeprazole14 in 1 BOTTLETABLET, DELAYED RELEASE147
43598-286-70Omeprazole7 in 1 BLISTER PACKTABLET, DELAYED RELEASE77
43598-286-74Omeprazole1 in 1 CARTONTABLET, DELAYED RELEASE17
43598-286-74Omeprazole14 in 1 BLISTER PACKTABLET, DELAYED RELEASE147

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43598-286OMEPRAZOLE TABLET, DELAYED RELEASE [DR. REDDYS LABORATORIES INC]7Current NDC, Legacy NDC, 11 package rows20241222_4b3b389d-a151-d851-cb05-64eb49979e5e.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
43598-286-33EA - Each43598-28642067ff0-a05a-4cf1-a797-5af13391fee412024-11-05
43598-286-52EA - Each43598-286df0c4c77-a812-44e6-add5-fb5148d2a50212024-11-05

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 5 of 134 · 2,676 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Eyewash Station Additive ConcentrateCHLORHEXIDINE GLUCONATE AND PROPYLENE GLYCOLGlobal Equipment Companybc93a1e8-aa3c-6735-e053-2995a90ad6e82026-07-16WarningsExact identifier
unii: 6DC9Q167V3
CalamineFERRIC OXIDE REDBetter Living Brands, LLCc7ef0ef3-6861-4b94-af4b-371fee8c1f3d2026-07-16Warnings, Adverse reactionsExact identifier
unii: 1K09F3G675
Revitalize Energizing Eye DropsNAPHAZOLINE HYDROCHLORIDE ,PROPYLENE GLYCOLRevitalize Energy Inc.518aac87-1642-4b2f-bca1-b74d21261eea2026-07-16WarningsExact identifier
unii: 6DC9Q167V3
OmeprazoleOMEPRAZOLEP & L Development, LLC883e428a-e157-4bbf-8657-e7a93dc99e8c2026-07-14WarningsExact identifier
rxcui: 402014
OmeprazoleOMEPRAZOLEWALMART INC. (see also Equate)d3c1ba08-680d-4e39-875c-1f1d42ae787c2026-07-13WarningsExact identifier
rxcui: 402014
OmeprazoleOMEPRAZOLEHAWAII REPACK, INC.9359e826-5263-44fc-8dd3-9d0852fe42d62026-07-13Warnings, Adverse reactionsExact identifier
unii: KG60484QX9
OmeprazoleOMEPRAZOLEBryant Ranch Prepackdcaadc8c-32d1-476f-b821-973c012b7fa72026-07-10Warnings, Adverse reactionsExact identifier
unii: KG60484QX9
Bombee Honey Daily Glow Shield SunscreenHOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDEABT ASIA Inc.56112dff-b091-7a56-e063-6294a90a77d32026-07-08WarningsExact identifier
unii: 15FIX9V2JP
Omeprazole, 24/7 Life by 7-ElevenOMEPRAZOLE TABLET, DELAYED RELEASELil' Drug Store Products, Inc.36d8a272-6cca-e759-e063-6394a90a9df82026-07-08WarningsExact identifier
rxcui: 402014
Stay Ageless Tinted Mineral SunscreenBROAD SPECTRUM SPF30DERMIO DERMATOLOGY LLC562f5b0d-6a10-305d-e063-6394a90a59802026-07-08WarningsExact identifier
unii: 15FIX9V2JP
Stay Ageless Tinted Mineral SunscreenBROAD SPECTRUM SPF30Suzanne's Skin2soul LLC562fbaa6-f93a-5ec4-e063-6294a90a96342026-07-08WarningsExact identifier
unii: 15FIX9V2JP
careone omeprazoleOMEPRAZOLEAmerican Sales Company5b88717a-e90c-4e74-ae2a-29270e14a3cc2026-07-08WarningsExact identifier
unii: KG60484QX9
Aussie Betta Tallow Sunscreen SPF50 SPF50TITANIUM DIOXIDE AND ZINC OXIDE SUNSCREENAUSSIE BETTA HEALTHY CARE PTY LTD56007d82-ff5b-6c26-e063-6294a90a09b62026-07-07WarningsExact identifier
unii: 15FIX9V2JP
Polyvinyl AlcoholPOLYVINYL ALCOHOLAvPAKf18b61da-4033-341a-e053-2a95a90a8ebf2026-07-07WarningsExact identifier
unii: 532B59J990
Artificial TearsARTIFICIAL TEARSAvPAKf18bebf2-1936-658f-e053-2a95a90a50122026-07-07WarningsExact identifier
unii: 3NXW29V3WO
EELHOE Body Coverage PerfectorTITANIUM DIOXIDEShantou Eelhoe Daily Chemical Technology Co., Ltd.5610c3b7-456b-3bc1-e063-6394a90a3fa82026-07-07WarningsExact identifier
unii: 15FIX9V2JP
Premier Tinted Mineral SunscreenBROAD SPECTRUM SPF30Emerald Aesthetics LLC55f88dd1-346c-22a5-e063-6294a90a711f2026-07-06WarningsExact identifier
unii: 15FIX9V2JP
clear laxPOLYETHYLENE GLYCOL 3350HyVee Inc5bcf01d8-ddf3-4e64-8d3f-3526a51a58592026-07-02WarningsExact identifier
unii: G2M7P15E5P
OHUI Ultimate Cover CC Cushion Compact 02 Natural BeigeTITANIUM DIOXIDELG H&H Co., Ltd.d307471c-6cc6-ce48-e053-2995a90a3e022026-07-02WarningsExact identifier
unii: 15FIX9V2JP
OmeprazoleOMEPRAZOLESt. Mary's Medical Park Pharmacy4c0cf466-f9e8-390e-e063-6294a90a2ed82026-07-02Warnings, Adverse reactionsExact identifier
unii: KG60484QX9

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.