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I 51 Pill - yellow oval, 8mm

Pill with imprint I 51 is Yellow, Oval and has been identified as Pantoprazole Sodium Delayed-Release 20 mg. It is supplied by Aurobindo Pharma Limited.

Pantoprazole is used in the treatment of Barrett's Esophagus; Erosive Esophagitis; Duodenal Ulcer; GERD; Gastritis/Duodenitis 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 Substances Act (CSA).

Images for I 51

Pantoprazole sodium delayed-release 20 mg I 51
Pantoprazole sodium delayed-release 20 mg I 51 Front
Pantoprazole sodium delayed-release 20 mg I 51 Back

Pantoprazole Sodium Delayed-Release

I 51
20 mg
8.00 mm
Prescription only
Drug Class
Proton pump inhibitors
Pregnancy Category
B - No proven risk in humans
CSA Schedule
Not a controlled drug
Labeler / Supplier
Aurobindo Pharma Limited
National Drug Code (NDC)
Inactive Ingredients
calcium stearate, ferric oxide yellow, hypromellose 2910 (3 mPa.s), mannitol, methacrylic acid - ethyl acrylate copolymer (1:1) type a, sodium carbonate, triethyl citrate, ammonia, ferrosoferric oxide, ferric oxide red, isopropyl alcohol, butyl alcohol, propylene glycol, shellac

Note: Inactive ingredients may vary.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.