FDA.reportPublic FDA data

up and up omeprazole

Product NDC
11673-212
11-digit product format
116730212
Labeler code
11673
Product ID
11673-212_1713a351-8a7a-405c-b37d-e01c2de0c246
Type
HUMAN OTC DRUG
Nonproprietary name
omeprazole
Dosage form
TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
Route
ORAL
Labeler
Target Corporation
Application
NDA209400
Marketing category
NDA
Marketing start
2018-05-09
Substance
OMEPRAZOLE
Active strength
20 mg/1
Pharmacologic classes
Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
up and up omeprazole
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OMEPRAZOLE20 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiKG60484QX9
Rxcui2003656

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
873ef493-6b37-49d8-ac7f-bfca4117d2c1Product name520210607
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
f33561b9-47cb-411c-a228-16c62e346cd4Product name120200415
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
ade821ba-260a-47e2-bd89-743e27ac9906Product name120161121
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-212-55up and up omeprazole14 in 1 CARTONTABLET, ORALLY DISINTEGRATING, D145
11673-212-55up and up omeprazole3 in 1 CARTONTABLET, ORALLY DISINTEGRATING, D35
11673-212-74up and up omeprazole1 in 1 BLISTER PACKTABLET, ORALLY DISINTEGRATING, D15
11673-212-74up and up omeprazole14 in 1 CARTONTABLET, ORALLY DISINTEGRATING, D145

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-212UP AND UP OMEPRAZOLE (OMEPRAZOLE) TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE [TARGET CORPORATION]5Current NDC, Legacy NDC, 4 package rows20250205_8f2eb5e8-80f2-4c40-a8ad-e1d9c10d0c56.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2003656omeprazole 20 MG Delayed Release Disintegrating Oral TabletPSN8f2eb5e8-80f2-4c40-a8ad-e1d9c10d0c565
2003656omeprazole 20 MG Disintegrating Oral TabletSCD8f2eb5e8-80f2-4c40-a8ad-e1d9c10d0c565
2003656omeprazole 20 MG (as omeprazole magnesium 20.6 MG) Delayed Release Disintegrating Oral TabletSY8f2eb5e8-80f2-4c40-a8ad-e1d9c10d0c565

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-212-55116730212553 CARTON in 1 CARTON (11673-212-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK3 carton2018-05-090000-00-00NoNoCurrent
11673-212-741167302127414 BLISTER PACK in 1 CARTON (11673-212-74) > 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK14 blister pack2018-05-090000-00-00NoNoCurrent