KU 181 (Pantoprazole sodium delayed release 40 mg)

Pill imprint KU 181 has been identified as Pantoprazole sodium delayed release 40 mg.

Pantoprazole is used in the treatment of barrett's esophagus; gerd; erosive esophagitis; duodenal ulcer; zollinger-ellison syndrome (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 subject to the Controlled Substances Act.

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Pantoprazole sodium delayed release 40 mg KU 181
Pantoprazole sodium delayed release 40 mg KU 181
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:
N - Not a controlled drug
Manufacturer:
Kremers Urban
National Drug Code (NDC):
62175-0181
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)

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