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; gerd; erosive esophagitis; duodenal ulcer; dumping 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 subject to the Controlled Substances Act.

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Pantoprazole sodium delayed release 20 mg P20
Pantoprazole sodium delayed release 20 mg P20
Pantoprazole sodium delayed release
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)
Other Manufacturers / Repackagers:
NDC CodeManufacturer / 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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