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; erosive esophagitis; dumping syndrome; 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 a controlled substance under the Controlled Substance Act (CSA).
- KU 181
- 40 mg
- Elliptical / Oval
- Prescription only
- Drug Class:
- Proton pump inhibitors
- Pregnancy Category:
- B - No proven risk in humans
- CSA Schedule:
- Not a controlled drug
- Kremers Urban
- National Drug Code (NDC):
- Inactive Ingredients:
- ferrosoferric oxide
methacrylic acid - methyl methacrylate copolymer (1:1)
Note: Inactive ingredients may vary.
|NDC Code||Manufacturer / Repackager|
|63739-0564||McKesson Packaging Services|
|68084-0006||Amerisource Health Services|
|68084-0657||Amerisource Health Services|
More about pantoprazole
- Side Effects
- During Pregnancy or Breastfeeding
- Dosage Information
- Drug Images
- Drug Interactions
- Support Group
- Pricing & Coupons
- En Español
- 114 Reviews – Add your own review/rating
- Drug class: proton pump inhibitors
- Pantoprazole delayed-release tablets
- Pantoprazole suspension
- Pantoprazole (Advanced Reading)
- Pantoprazole Intravenous (Advanced Reading)
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