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KU 180 (Pantoprazole sodium delayed release 20 mg)

This pill with imprint "KU 180" is White, Elliptical / Oval and has been identified as Pantoprazole sodium delayed release 20 mg. It is manufactured by Kremers Urban.

Pantoprazole is used in the treatment of barrett's esophagus; dumping syndrome; zollinger-ellison syndrome; gerd; erosive esophagitis (and more), and belongs to the drug class proton pump inhibitors. There is no proven risk in humans during pregnancy. Pantoprazole 20 mg is not a controlled substance under the Controlled Substance Act (CSA).

Pantoprazole sodium delayed release 20 mg KU 180
Pantoprazole sodium delayed release 20 mg KU 180
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Pantoprazole sodium delayed release
KU 180
20 mg
Elliptical / Oval
Prescription only
Drug Class:
Proton pump inhibitors
Pregnancy Category:
B - No proven risk in humans
CSA Schedule:
Not a controlled drug
Kremers Urban
National Drug Code (NDC):
Inactive Ingredients:
ferrosoferric oxide
glyceryl dibehenate
isopropyl alcohol
lactose monohydrate
propylene glycol
magnesium silicate
titanium dioxide
triethyl citrate
methacrylic acid - methyl methacrylate copolymer (1:1)

Note: Inactive ingredients may vary.

Imprint Code FAQ's

Other Manufacturers / Repackagers:
NDC CodeManufacturer / Repackager
68084-0643 Amerisource Health Services

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Disclaimer: Every effort has been made to ensure that the information provided is accurate, up-to-date, and complete, but no guarantee is made to that effect. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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