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; gerd; dumping syndrome; 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).

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Pantoprazole Sodium Delayed Release

Imprint:

KU 181

Strength:

40 mg

Color:

White

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.

Other Labelers / Repackagers:

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

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