Skip to Content
Print Save

KU 415 (Lansoprazole Delayed-Release 15 mg)

Pill with imprint KU 415 is Purple / White, Capsule-shape and has been identified as Lansoprazole Delayed-Release 15 mg. It is supplied by Lannett Company, Inc..

Lansoprazole is used in the treatment of barrett's esophagus; duodenal ulcer; duodenal ulcer prophylaxis; gerd; erosive esophagitis and belongs to the drug class proton pump inhibitors. There is no proven risk in humans during pregnancy. Lansoprazole 15 mg is not a controlled substance under the Controlled Substances Act (CSA).

Images for KU 415

Lansoprazole delayed-release 15 mg KU 415
Lansoprazole delayed-release 15 mg KU 415

Save up to 80% off prescription medications

Click here for your free Discount Card

Lansoprazole Delayed-Release

Imprint
KU 415
Strength
15 mg
Color
Purple / White
Size
16.00 mm
Shape
Capsule-shape
Availability
Rx and/or OTC
Drug Class
Proton pump inhibitors
Pregnancy Category
B - No proven risk in humans
CSA Schedule
Not a controlled drug
Labeler / Supplier
Lannett Company, Inc.
National Drug Code (NDC)
62175-0415
Inactive Ingredients
FD&C Blue No. 1, FD&C Red No. 3, gelatin, hypromellose 2910 (6 mPa.s), magnesium carbonate, mannitol, methacrylic acid - ethyl acrylate copolymer (1:1) type a, polyethylene glycol 6000, polysorbate 80, sodium lauryl sulfate, sodium starch glycolate type A corn, magnesium silicate, titanium dioxide, shellac, isopropyl alcohol, butyl alcohol, ammonia, alcohol, ferrosoferric oxide, aluminum chlorohydrex propylene glycol

Note: Inactive ingredients may vary.

More Info Imprint Search Print

Get help with Imprint Code FAQs.

Further information

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

Medical Disclaimer