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KU 181 (Pantoprazole sodium delayed release 40 mg)

Pill imprint KU 181 has been identified as Pantoprazole sodium delayed release 40 mg.

Pantoprazole is used in the treatment of barrett's esophagus; erosive esophagitis; gerd; dumping syndrome; duodenal ulcer (and more), and belongs to the drug class proton pump inhibitors. There is no proven risk in humans during pregnancy. Pantoprazole 40 mg is not a controlled substance under the Controlled Substance Act (CSA).

Pantoprazole sodium delayed release 40 mg KU 181
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Pantoprazole sodium delayed release
KU 181
40 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
63739-0564 McKesson Packaging Services
68084-0006 Amerisource Health Services
68084-0657 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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