NDC 11673-212

up and up omeprazole

Omeprazole

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

Product ID11673-212_3511d713-1cc2-4648-a070-695b2a89b9a2
NDC11673-212
Product TypeHuman Otc Drug
Proprietary Nameup and up omeprazole
Generic NameOmeprazole
Dosage FormTablet, Orally Disintegrating, Delayed Release
Route of AdministrationORAL
Marketing Start Date2018-05-09
Marketing CategoryNDA / NDA
Application NumberNDA209400
Labeler NameTarget Corporation
Substance NameOMEPRAZOLE
Active Ingredient Strength20 mg/1
Pharm ClassesCytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 11673-212-55

3 CARTON in 1 CARTON (11673-212-55) > 14 BLISTER PACK in 1 CARTON > 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK
Marketing Start Date2018-05-09
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 11673-212-74 [11673021274]

up and up omeprazole TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
Marketing CategoryNDA
Application NumberNDA209400
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-05-09

NDC 11673-212-55 [11673021255]

up and up omeprazole TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
Marketing CategoryNDA
Application NumberNDA209400
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-05-09

Drug Details

Active Ingredients

IngredientStrength
OMEPRAZOLE20 mg/1

OpenFDA Data

SPL SET ID:8f2eb5e8-80f2-4c40-a8ad-e1d9c10d0c56
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 2003656
  • 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

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.