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KU 820 (Esomeprazole Magnesium Delayed-Release 20 mg)

Pill with imprint KU 820 is Blue & White, Capsule-shape and has been identified as Esomeprazole Magnesium Delayed-Release 20 mg. It is supplied by Lannett Company, Inc..

Esomeprazole is used in the treatment of barrett's esophagus; gerd; erosive esophagitis; duodenal ulcer prophylaxis; gastric ulcer prophylaxis and belongs to the drug class proton pump inhibitors. Risk cannot be ruled out during pregnancy. Esomeprazole 20 mg is not a controlled substance under the Controlled Substances Act (CSA).

Images for KU 820

Esomeprazole magnesium delayed-release 20 mg KU 820

Esomeprazole Magnesium Delayed-Release

Imprint
KU 820
Strength
20 mg
Color
Blue & White
Size
14.00 mm
Shape
Capsule-shape
Availability
Rx and/or OTC
Drug Class
Proton pump inhibitors
Pregnancy Category
C - Risk cannot be ruled out
CSA Schedule
Not a controlled drug
Labeler / Supplier
Lannett Company, Inc.
National Drug Code (NDC)
62175-0820
Inactive Ingredients
hypromellose 2208 (100 mPa.s), magnesium stearate, methacrylic acid - ethyl acrylate copolymer (1:1) type a, polysorbate 80, magnesium silicate, triethyl citrate, gelatin, FD&C Blue No. 1, sodium lauryl sulfate, titanium dioxide, FD&C Red No. 40, propylene glycol, shellac, potassium hydroxide, isopropyl alcohol, alcohol, butyl alcohol

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.