NDC 11673-915

up and up omeprazole

Omeprazole

up and up omeprazole is a Oral Tablet, Delayed Release in the Human Otc Drug category. It is labeled and distributed by Target Corporation. The primary component is Omeprazole.

Product ID11673-915_4086f86a-772e-4316-982c-c0febb433a96
NDC11673-915
Product TypeHuman Otc Drug
Proprietary Nameup and up omeprazole
Generic NameOmeprazole
Dosage FormTablet, Delayed Release
Route of AdministrationORAL
Marketing Start Date2009-07-14
Marketing CategoryNDA / NDA
Application NumberNDA022032
Labeler NameTarget Corporation
Substance NameOMEPRAZOLE
Active Ingredient Strength20 mg/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 11673-915-01

1 BOTTLE in 1 CARTON (11673-915-01) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE
Marketing Start Date2013-08-13
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 11673-915-30 [11673091530]

up and up omeprazole TABLET, DELAYED RELEASE
Marketing CategoryNDA
Application NumberNDA022032
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2009-07-14
Marketing End Date2015-03-01

NDC 11673-915-55 [11673091555]

up and up omeprazole TABLET, DELAYED RELEASE
Marketing CategoryNDA
Application NumberNDA022032
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2009-07-14
Marketing End Date2015-02-01

NDC 11673-915-03 [11673091503]

up and up omeprazole TABLET, DELAYED RELEASE
Marketing CategoryNDA
Application NumberNDA022032
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2013-08-14

NDC 11673-915-74 [11673091574]

up and up omeprazole TABLET, DELAYED RELEASE
Marketing CategoryNDA
Application NumberNDA022032
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2009-07-20
Marketing End Date2015-02-01

NDC 11673-915-01 [11673091501]

up and up omeprazole TABLET, DELAYED RELEASE
Marketing CategoryNDA
Application NumberNDA022032
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-08-13

NDC 11673-915-02 [11673091502]

up and up omeprazole TABLET, DELAYED RELEASE
Marketing CategoryNDA
Application NumberNDA022032
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-02-27
Marketing End Date2020-01-01

Drug Details

Active Ingredients

IngredientStrength
OMEPRAZOLE20 mg/1

OpenFDA Data

SPL SET ID:2f2b26fe-dbc2-4185-8a27-6b166dd49ba2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 402014

    • NDC Crossover Matching brand name "up and up omeprazole" or generic name "Omeprazole"

    NDCBrand NameGeneric Name
    11673-018up and up omeprazoleup and up omeprazole
    11673-212up and up omeprazoleup and up omeprazole
    11673-915up and up omeprazoleup and up omeprazole
    0363-1008Acid ReducerOmeprazole
    0536-1322Acid ReducerOmeprazole
    0113-7401Basic Care OmeprazoleOmeprazole
    0113-7520basic care omeprazoleomeprazole
    0113-7915Basic Care OmeprazoleOmeprazole
    0113-0520good sense omeprazoleomeprazole
    0113-0915Good Sense OmeprazoleOmeprazole
    0113-1723Good Sense OmeprazoleOmeprazole
    0113-1803good sense omeprazole delayed releaseomeprazole
    0093-5294OmeprazoleOmeprazole
    0363-0007omeprazoleOmeprazole
    0363-0915omeprazoleOmeprazole
    0363-1607OmeprazoleOmeprazole
    0363-1819omeprazoleomeprazole
    0378-5211Omeprazoleomeprazole
    0378-5222Omeprazoleomeprazole
    0378-6150Omeprazoleomeprazole
    0615-1359OmeprazoleOmeprazole
    0615-2302OmeprazoleOmeprazole
    0615-2305OmeprazoleOmeprazole
    0615-7933OmeprazoleOmeprazole
    0615-8079OmeprazoleOmeprazole
    0615-8320OmeprazoleOmeprazole
    0615-8406OmeprazoleOmeprazole
    0781-2234OmeprazoleOmeprazole
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