Lansoprazole capsule, delayed release

Active ingredient(s)

Lansoprazole USP, 15 mg

Purpose

Acid reducer

Use(s)

  • treats frequent heartburn (occurs 2 or moredays a week)
  • not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Warnings

Allergy alert:Do not use if you are allergic to lansoprazole

Do not use

  • if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools.These may be signs of a serious condition. See your doctor.

Ask a doctor before use if you have

  • liver disease
  • had heartburn over 3 months. This may be a sign of a more serious condition.
  • heartburn with lightheadedness, sweating or dizziness
  • chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness
  • frequent chest pain
  • frequent wheezing, particularly with heartburn
  • unexplained weight loss
  • nausea or vomiting
  • stomach pain

Ask a doctor or pharmacist before use if you are taking

  • warfarin (blood-thinning medicine)
  • prescription antifungal or anti-yeast medicines
  • digoxin (heart medicine)
  • theophylline (asthma medicine)
  • tacrolimus (immune system medicine)
  • atazanavir (medicine for HIV infection)

Stop use and ask doctor if

  • your heartburn continues or worsens
  • you need to take this product for more than 14 days
  • you need to take more than 1 course of treatment every 4 months
  • you get diarrhea

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

  • adults 18 years of age and older
  • this product is to be used once a day (every 24 hours), every day for 14 days
  • it may take 1 to 4 days for full effect, although some people get complete relief of symptoms within 24 hours

14-Day Course of Treatment

  • swallow 1 capsule with a glass of water before eating in the morning
  • take every day for 14 days
  • do not take more than 1 capsule a days
  • swallow whole. Do not crush or chew capsules.
  • do not use for more than 14 days unless directed by your doctor

Repeated 14-Day Courses (if needed)

  • you may repeat a 14-day course every 4 months
  • do not take for more than 14 days or more often than every 4 months unless directed by a doctor
  • children under 18 years of age: ask a doctor before use. Heartburn in children may sometimes be caused by a serious condition.

Other information

  • read the directions, warnings and package insert before use
  • keep the carton and package insert. They contain important information.
  • store at 20 25C (68 77 F)
  • keep product out of high heat and humidity
  • protect product from moisture

Inactive ingredients

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

Questions or comments?

call 1-888-375-3784

Manufactured by:

Dr. Reddys Laboratories Limited

Bachupally - 500 090 INDIA

Ingredients and appearance - Product information

Lansoprazole capsule, delayed release- Lansoprazole

Product information

Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC: 49035-739
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Lansoprazole ( UNII: 0K5C5T2QPG)( Lansoprazole - UNII: 0K5C5T2QPG ) 15 mgin 1

Inactive Ingredients

Ingredient Name Code
Fd&c blue no. 2 ( UNII: L06K8R7DQK)
Ferric oxide red ( UNII: 1K09F3G675)
Ferric oxide yellow ( UNII: EX438O2MRT)
Gelatin ( UNII: 2G86QN327L)
Hydroxypropyl cellulose ( UNII: RFW2ET671P)
Ferrosoferric oxide ( UNII: XM0M87F357)
Hydroxypropyl cellulose, low substituted ( UNII: 2165RE0K14)
Magnesium carbonate ( UNII: 0E53J927NA)
Methacrylic acid - ethyl acrylate copolymer (1:1) type a ( UNII: NX76LV5T8J)
Polyethylene glycol 6000 ( UNII: 30IQX730WE)
Polysorbate 80 ( UNII: 6OZP39ZG8H)
Sodium lauryl sulfate ( UNII: 368GB5141J)
Starch, corn ( UNII: O8232NY3SJ)
Sucrose ( UNII: C151H8M554)
Talc ( UNII: 7SEV7J4R1U)
Titanium dioxide ( UNII: 15FIX9V2JP)

Product Characteristics

Shape CAPSULE Score 1
Size 3 mm Imprint Code RDY;398
Color GREEN (opaque green colored body)

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
ANDA ANDA202194 USA

Labeler - Wal-Mart Stores Inc( 051957769)

Establishment

Name ID/FEI Business Operations
Wal-Mart Stores Inc 051957769 analysis( 49035-739), manufacture( 49035-739)

Principal display panel

Container carton : 14's count

carton