Active Ingredient(S)
Lansoprazole USP, 15 mg
The following Structured Product Label (SPL) was submitted to the FDA by Dr. Reddy's Laboratories Limited for the product Lansoprazole (NDC 55111-739). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient(s), purpose, use(s), warnings, do not use, ask a doctor before use if you have, ask a doctor or pharmacist before use if you are taking, stop use and ask doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Lansoprazole USP, 15 mg
Acid reducer
Allergy alert: Do not use if you are allergic to lansoprazole
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
14-Day Course of Treatment
Repeated 14-Day Courses (if needed)
FD&C Blue No. 2, gelatin, hydroxypropyl cellulose, iron oxide black, iron oxide red, iron oxide yellow, low substituted hydroxypropyl cellulose, magnesium carbonate, methacrylic acid copolymer, polyethylene glycol 6000, polysorbate 80, sodium lauryl sulphate, starch (corn), sucrose, sugar spheres, talc, titanium dioxide
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Manufactured by:
Dr. Reddy’s Laboratories Limited
Bachupally - 500 090 INDIA
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