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 stomach ulcer; gerd; barrett's esophagus; peptic ulcer; 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 subject to the Controlled Substances Act.
See also related documents.
Images for P20 (Pantoprazole sodium delayed release 20 mg)
- Imprint:
-
P20
- Strength:
- 20 mg
- Color:
- Yellow
- Shape:
- Elliptical / Oval
- Availability:
- Prescription only
- Drug Class:
- Proton pump inhibitors
- Pregnancy Category:
- B - No proven risk in humans
- CSA Schedule:
- N - Not a controlled drug
- Manufacturer:
- Wyeth Pharmaceuticals
- National Drug Code (NDC):
- 00008-0606
- Inactive Ingredients:
- calcium stearate
crospovidone
ferric oxide yellow
mannitol
methacrylic acid - ethyl acrylate copolymer (1:1) type a
polysorbate 80
povidone k25
povidone k90
propylene glycol
sodium carbonate
sodium lauryl sulfate
titanium dioxide
triethyl citrate
hypromellose 2208 (100 mPa.s)
| NDC Code | Manufacturer / Repackager |
|---|---|
| 00008-0843 | Wyeth |
| 16590-0939 | Stat RX USA LLC (repackager) |
| 54868-4786 | Physicians Total Care Inc (repackager) |
| 68115-0687 | Dispensexpress Inc (repackager) |
| 49999-0755 | Lake Erie Medical and Surgical Supply (repackager) |
| 58016-0072 | Southwood Pharmaceuticals Inc (repackager) |
| 16590-0635 | Stat RX USA LLC (repackager) |
| 54868-6038 | Physicians Total Care Inc (repackager) |
Note: Inactive ingredients may vary.
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Pantoprazole sodium delayed release is associated with the treatment of:
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