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Lansoprazole - Medication Information

Product NDC Code 71335-9694
Drug Name

Lansoprazole

Type Generic
Pharm Class Inhibition Gastric Acid Secretion [PE],
Proton Pump Inhibitor [EPC],
Proton Pump Inhibitors [MoA]
Active Ingredients
Lansoprazole 15 mg/1
Route ORAL
Dosage Form CAPSULE, DELAYED RELEASE
RxCUI drug identifier 596843
Application Number ANDA203306
Labeler Name Bryant Ranch Prepack
Packages
Package NDC Code Description
71335-9694-1 30 capsule, delayed release in 1 bottle (71335-9694-1)
71335-9694-2 15 capsule, delayed release in 1 bottle (71335-9694-2)
71335-9694-3 60 capsule, delayed release in 1 bottle (71335-9694-3)
71335-9694-4 90 capsule, delayed release in 1 bottle (71335-9694-4)
71335-9694-5 28 capsule, delayed release in 1 bottle (71335-9694-5)
Check if available Online

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient (in each capsule) Lansoprazole 15 mg

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
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 day 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.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients acetone, D&C Red No. 28, D&C Yellow No. 10, FD&C Blue No. 1,gelatin, hypromellose, isopropyl alcohol, light magnesium carbonate, methacrylic acid copolymer type C, polyethylene glycol, polysorbate 80, sugar spheres (contain sucrose and starch), talc, titanium dioxide. Printing Ink contains butyl alcohol, dehydrated alcohol isopropyl alcohol, potassium hydroxide, propylene glycol, purified water, shellac, strong ammonia solution, titanium dioxide Questions or comments? 1-844-874-7464

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Purpose

Information about the drug product’s indications for use.
Purpose Acid reducer

Spl product data elements

Usually a list of ingredients in a drug product.
Lansoprazole Lansoprazole LANSOPRAZOLE LANSOPRAZOLE ACETONE D&C RED NO. 28 D&C YELLOW NO. 10 FD&C BLUE NO. 1 GELATIN, UNSPECIFIED HYPROMELLOSE, UNSPECIFIED ISOPROPYL ALCOHOL MAGNESIUM CARBONATE METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A POLYSORBATE 80 SUCROSE TALC TITANIUM DIOXIDE POLYETHYLENE GLYCOL, UNSPECIFIED BUTYL ALCOHOL ALCOHOL POTASSIUM HYDROXIDE PROPYLENE GLYCOL WATER SHELLAC AMMONIA

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Lansoprazole DR 15mg Capsule (OTC) Label

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
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 doctor or pharmacist

Information about when a doctor or pharmacist should be consulted about drug/drug or drug/food interactions before using a drug product.
Ask a doctor or pharmacist before use if you are taking a prescription drug. Acid reducers may interact with certain prescription drugs.

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
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.

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
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).

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
Stop use and ask a 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 you develop a rash or joint pain

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast-feeding, ask a health professional before use.

How supplied

Information about the available dosage forms to which the labeling applies, and for which the manufacturer or distributor is responsible. This field ordinarily includes the strength of the dosage form (in metric units), the units in which the dosage form is available for prescribing, appropriate information to facilitate identification of the dosage forms (such as shape, color, coating, scoring, and National Drug Code), and special handling and storage condition information.
HOW SUPPLIED NDC: 71335-9694-1: 30 Capsules in a BOTTLE NDC: 71335-9694-2: 15 Capsules in a BOTTLE NDC: 71335-9694-3: 60 Capsules in a BOTTLE NDC: 71335-9694-4: 90 Capsules in a BOTTLE NDC: 71335-9694-5: 28 Capsules in a BOTTLE

Storage and handling

Information about safe storage and handling of the drug product.
Other information read the directions, warnings and package insert before use keep the package and package insert. They contain important information. store at 20-25°C (68-77°F) keep product out of high heat and humidity protect product from moisture close cap tightly after use Inactive ingredients acetone, D&C Red No. 28, D&C Yellow No. 10, FD&C Blue No. 1,gelatin, hypromellose, isopropyl alcohol, light magnesium carbonate, methacrylic acid copolymer type C, polyethylene glycol, polysorbate 80, sugar spheres (contain sucrose and starch), talc, titanium dioxide. Printing Ink contains butyl alcohol, dehydrated alcohol isopropyl alcohol, potassium hydroxide, propylene glycol, purified water, shellac, strong ammonia solution, titanium dioxide Questions or comments? 1-844-874-7464 PATIENT INFORMATION Treats Frequent Heartburn Lansoprazole (lan-SO-pruh-zole) Delayed-Release Capsules USP, 15 mg / Acid Reducer May take 1 to 4 days for full effect Sodium Free Please read the entire package insert before taking Lansoprazole Delayed-Release Capsules, USP Save for future reference. How Lansoprazole Delayed-Release Capsules, USP Treat Your Frequent Heartburn Lansoprazole delayed-release capsules, USP stop acid production at the source - the pumps that release acid into the stomach. Lansoprazole delayed-release capsules, USP are taken once a day (every 24 hours), every day for 14 days. What You Can Expect When Taking Lansoprazole Delayed-Release Capsules, USP Frequent heartburn can occur anytime during the 24-hour period (day or night). Take lansoprazole delayed-release capsules, USP in the morning before eating. Lansoprazole delayed-release capsules, USP are clinically proven to treat frequent heartburn. Although some people get complete relief of symptoms within 24 hours, it may take 1 to 4 days for full effect. Make sure you take lansoprazole delayed-release capsules, USP every day for 14 days to treat your frequent heartburn. Who Should Take Lansoprazole Delayed-Release Capsules, USP Adults (18 years and older) with frequent heartburn - when you have heartburn 2 or more days a week. Who Should NOT Take Lansoprazole Delayed-Release Capsules, USP People who have one episode of heartburn a week or less, or who want immediate relief of heartburn. How to Take Lansoprazole Delayed-Release Capsules, USP 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 day. Swallow whole. Do not crush or chew capsules. Do not use for more than 14 days unless directed by your doctor. When to Take Lansoprazole Delayed-Release Capsules, USP Again You may repeat a 14-day course of therapy every 4 months. When to Talk to Your Doctor Do not take for more than 14 days or more often than every 4 months unless directed by a doctor. Warnings and When to Ask Your Doctor 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 a prescription drug. Acid reducers may interact with certain prescription drugs. Stop use ask a 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 you develop a rash or joint pain 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 at 1-800-222-1222. Tips for Managing Heartburn Avoid foods or drinks that are more likely to cause heartburn, such as rich, spicy, fatty and fried foods, chocolate, caffeine, alcohol and even some acidic fruits and vegetables. Eat slowly and do not eat big meals. Do not eat late at night or just before bedtime. Do not lie flat or bend over soon after eating. Raise the head of your bed. Wear loose-fitting clothing around your stomach. If you are overweight, lose weight. If you smoke, quit smoking. Clinical studies prove Lansoprazole Delayed-Release Capsules, USP effectively treats frequent heartburn In three clinical studies, lansoprazole delayed-release capsules, USP were shown to be significantly better than placebo in treating frequent heartburn. How Lansoprazole Delayed-Release Capsules, USP are Sold Lansoprazole delayed-release capsules, USP are available in 14 capsules, 28 capsules and 42 capsule sizes. These sizes contain one, two and three 14-day courses of treatment, respectively. Do not use for more than 14 days in a row unless directed by your doctor. For the 28 count (two 14-day courses) and the 42 count (three 14-day courses), you may repeat a 14-day course every 4 months. For Questions or Comments About Lansoprazole Delayed-Release Capsules, USP Call 1-844-474-7464 Manufactured by: Natco Pharma Limited Kothur - 509 228, India Distributed by: Rising Pharma Holdings, Inc. East Brunswick, NJ 08816 Revised: 11/2020

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings Allergy alert: Do not use if you are allergic to lansoprazole

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API