P20 (Pantoprazole sodium delayed release 20 mg)
Pill imprint P20 has been identified as Pantoprazole sodium delayed release 20 mg.
Pantoprazole is used in the treatment of barrett's esophagus; erosive esophagitis; gastritis/duodenitis; dumping syndrome; zollinger-ellison syndrome (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).
- 20 mg
- Elliptical / Oval
- Prescription only
- Drug Class:
- Proton pump inhibitors
- Pregnancy Category:
- B - No proven risk in humans
- CSA Schedule:
- Not a controlled drug
- Wyeth Pharmaceuticals
- National Drug Code (NDC):
- Inactive Ingredients:
- calcium stearate
ferric oxide yellow
methacrylic acid - ethyl acrylate copolymer (1:1) type a
sodium lauryl sulfate
hypromellose 2208 (100 mPa.s)
|NDC Code||Manufacturer / Repackager|
|54868-4786||Physicians Total Care Inc (repackager)|
|49999-0755||Lake Erie Medical and Surgical Supply (repackager)|
|16590-0635||Stat RX USA LLC (repackager)|
|54868-6038||Physicians Total Care Inc (repackager)|
|16590-0939||Stat RX USA LLC (repackager)|
Note: Inactive ingredients may vary.
More about pantoprazole
- Pantoprazole delayed-release tablets
- Pantoprazole suspension
- Pantoprazole (Advanced Reading)
- Pantoprazole Intravenous (Advanced Reading)
Related treatment guides
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