KU 181 Pill: white, oval, 12mm
The pill with imprint KU 181 (White, Oval, 12mm) has been identified as Pantoprazole Sodium Delayed Release 40 mg and is used for Barrett's Esophagus, Erosive Esophagitis, Duodenal Ulcer, GERD, and Gastritis/Duodenitis. It belongs to the drug class proton pump inhibitors and is not a controlled substance.
Images for KU 181
Pantoprazole Sodium Delayed Release
- Imprint
- KU 181
- Strength
- 40 mg
- Color
- White
- Size
- 12.00 mm
- Shape
- 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.
Labelers / Repackagers
| NDC Code | Labeler / Repackager |
|---|---|
| 62175-0181 (Discontinued) | Kremers Urban Pharmaceuticals Inc. |
| 63739-0564 | McKesson Packaging Services |
| 68084-0657 (Discontinued) | Amerisource Health Services |
See also:
More about pantoprazole
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- Pantoprazole monograph
- Pantoprazole (FDA)
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- Pantoprazole Injection (FDA)
- Pantoprazole Oral Suspension (FDA)
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Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.