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KU 180 (Pantoprazole sodium delayed release 20 mg)

Pill imprint KU 180 has been identified as Pantoprazole sodium delayed release 20 mg.

Pantoprazole is used in the treatment of barrett's esophagus; gerd; dumping syndrome; erosive esophagitis; duodenal ulcer (and more), and belongs to the drug class proton pump inhibitors. There is no proven risk in humans during pregnancy. Pantoprazole 20 mg is not a controlled substance under the Controlled Substance Act (CSA).

Pantoprazole sodium delayed release 20 mg KU 180
Pantoprazole sodium delayed release 20 mg KU 180
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Pantoprazole sodium delayed release
Imprint:
KU 180
Strength:
20 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
Manufacturer:
Kremers Urban
National Drug Code (NDC):
62175-0180
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)
Other Manufacturers / Repackagers:
NDC CodeManufacturer / Repackager
68084-0643 Amerisource Health Services

Note: Inactive ingredients may vary.

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