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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; 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

KU 181
40 mg
12.00 mm
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, 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 CodeLabeler / Repackager
62175-0181 Kremers Urban Pharmaceuticals Inc.
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.