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KU 181 (Pantoprazole Sodium Delayed Release 40 mg)

Pill with imprint KU 181 is White, Elliptical / Oval and has been identified as Pantoprazole Sodium Delayed Release 40 mg. It is supplied by Kremers Urban.

Pantoprazole is used in the treatment of barrett's esophagus; dumping syndrome; gerd; duodenal ulcer; erosive esophagitis (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 Substances Act (CSA).

Images for KU 181

Pantoprazole sodium delayed release 40 mg KU 181

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
Labeler / Supplier:
Kremers Urban
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.

Other Labelers / Repackagers:

NDC CodeLabeler / Repackager
63739-0564 McKesson Packaging Services
68084-0657 Amerisource Health Services

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.