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KU 181 Pill - white oval, 12mm

Pill with imprint KU 181 is White, 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; erosive esophagitis; duodenal ulcer; gerd; gastritis/duodenitis 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 40 mg KU 181

Pantoprazole Sodium Delayed Release

KU 181
40 mg
12.00 mm
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, crospovidone, glyceryl dibehenate, hypromelloses, isopropyl alcohol, lactose monohydrate, propylene glycol, magnesium silicate, titanium dioxide, triethyl citrate, methacrylic acid - methyl methacrylate copolymer (1:1)

Note: Inactive ingredients may vary.

Labelers / Repackagers

NDC Code Labeler / Repackager
62175-0181 (Discontinued) Kremers Urban Pharmaceuticals Inc.
63739-0564 McKesson Packaging Services
68084-0657 (Discontinued) 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.