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).

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Pantoprazole Sodium Delayed Release

Imprint

KU 181

Strength

40 mg

Color

White

Size

12.00 mm

Shape

Elliptical / Oval

Availability

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	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.

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