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; 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 40 mg is not a controlled substance under the Controlled Substance Act (CSA).
- 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
- 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)
| NDC Code | Manufacturer / Repackager |
|---|---|
| 63739-0564 | McKesson Packaging Services |
| 68084-0006 | Amerisource Health Services |
| 68084-0657 | Amerisource Health Services |
Note: Inactive ingredients may vary.
More about pantoprazole
Consumer resources
- Pantoprazole,
- Pantoprazole
- Pantoprazole delayed-release tablets
- Pantoprazole suspension
- Pantoprazole (Advanced Reading)
- Pantoprazole Intravenous (Advanced Reading)
- Other brands: Protonix, Protonix IV
Professional resources
Related treatment guides
Disclaimer:
Every effort has been made to ensure that the information provided is accurate, up-to-date, and complete, but no guarantee is made to that effect. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.
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