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NDC 51660-0027-14 Esomeprazole 20 mg/1 Details
Esomeprazole 20 mg/1
Esomeprazole is a ORAL CAPSULE, DELAYED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by Ohm Laboratories Inc.. The primary component is ESOMEPRAZOLE MAGNESIUM.
MedlinePlus Drug Summary
Prescription esomeprazole is used to treat the symptoms of gastroesophageal reflux disease (GERD), a condition in which backward flow of acid from the stomach causes heartburn and possible injury of the esophagus (the tube between the throat and stomach) in adults and children 1 year of age and older. Prescription esomeprazole is used to treat damage from GERD in adults and children 1 month of age and older. Prescription esomeprazole is used to allow the esophagus to heal and prevent further damage to the esophagus in adults with GERD. Prescription esomeprazole is also used to decrease the chance that people who are taking nonsteroidal anti-inflammatory drugs (NSAIDs) will develop ulcers (sores in the lining of the stomach or intestine) in adults. It is also used with other medications to treat and prevent the return of stomach ulcers caused by a certain type of bacteria (H. pylori) in adults. Prescription esomeprazole is also used to treat conditions in which the stomach produces too much acid such as Zollinger-Ellison syndrome in adults. Nonprescription (over-the-counter) esomeprazole is used to treat frequent heartburn (heartburn that occurs at least 2 or more days a week) in adults. Esomeprazole is in a class of medications called proton pump inhibitors. It works by decreasing the amount of acid made in the stomach.
Related Packages: 51660-0027-14Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Esomeprazole
Product Information
| NDC | 51660-0027 |
|---|---|
| Product ID | 51660-027_df9b1217-4941-448a-9225-7c0684c141ff |
| Associated GPIs | |
| GCN Sequence Number | 047525 |
| GCN Sequence Number Description | esomeprazole magnesium CAPSULE DR 20 MG ORAL |
| HIC3 | D4J |
| HIC3 Description | PROTON-PUMP INHIBITORS |
| GCN | 12867 |
| HICL Sequence Number | 021607 |
| HICL Sequence Number Description | ESOMEPRAZOLE MAGNESIUM |
| Brand/Generic | Generic |
| Proprietary Name | Esomeprazole |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | esomeprazole magnesium |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | CAPSULE, DELAYED RELEASE |
| Route | ORAL |
| Active Ingredient Strength | 20 |
| Active Ingredient Units | mg/1 |
| Substance Name | ESOMEPRAZOLE MAGNESIUM |
| Labeler Name | Ohm Laboratories Inc. |
| Pharmaceutical Class | Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA212866 |
| Listing Certified Through | 2024-12-31 |
Package
Package Images
NDC 51660-0027-14 (51660002714)
| NDC Package Code | 51660-027-14 |
|---|---|
| Billing NDC | 51660002714 |
| Package | 1 BOTTLE in 1 CARTON (51660-027-14) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
| Marketing Start Date | 2020-08-14 |
| NDC Exclude Flag | N |
| Pricing Information | |
| Price Per Unit | 0.34279 |
| Pricing Unit | EA |
| Effective Date | 2024-02-21 |
| NDC Description | ESOMEPRAZOLE MAG DR 20 MG CAP |
| Pharmacy Type Indicator | C/I |
| OTC | Y |
| Explanation Code | 1 |
| Classification for Rate Setting | G |
| As of Date | 2024-02-21 |
Standard Product Labeling (SPL)/Prescribing Information SPL e6d19b0a-44a8-42fe-8a6c-717ecb3ac1c4 Details
Active ingredient (in each capsule)
Use
Warnings
Allergy alert:
- ▪
- Do not use if you are allergic to esomeprazole
- ▪
- Esomeprazole may cause severe skin reactions. Symptoms include:
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- If an allergic reaction occurs, stop use and seek medical help right away.
Do not use if you have:
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- trouble or pain swallowing food, vomiting with blood, or bloody or black stools
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- 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
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- frequent chest pain
These may be signs of a serious condition. See your doctor.
Ask a doctor or pharmacist before use if you are
Stop use and ask a doctor if
Keep out of reach of children.
Directions
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- adults 18 years of age and older
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- this product is to be used once a day (every 24 hours), every day for 14 days
- •
- may take 1 to 4 days for full effect
14-Day Course of Treatment
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- swallow 1 capsule with a glass of water before eating in the morning
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- take every day for 14 days
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- do not take more than 1 capsule a day
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- swallow whole. Do not crush or chew capsules.
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- 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
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- do not take for more than 14 days or more often than every 4 months unless directed by a doctor
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- children under 18 years of age: ask a doctor before use. Heartburn in children may sometimes be caused by a serious condition.
Other information
Inactive Ingredients
FD & C blue no 1, FD & C red no 3, ferrosoferric oxide, gelatin, hydroxypropyl cellulose, hypromellose, magnesium stearate, methacrylic acid copolymer dispersion, mono and di glycerides, polysorbate 80, potassium hydroxide, propylene glycol, shellac, sugar spheres (corn starch and sucrose), talc, titanium dioxide and triethyl citrate.
Questions?
Call toll-free weekdays 8:30 AM to 5 PM EST at 1-800-818-4555.
TAMPER-EVIDENT FEATURES: Do not use if seal under bottle cap imprinted with "SEALED for YOUR PROTECTION" or blue band around center of each capsule is broken or missing.
Tips for Managing Heartburn
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- 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.
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- Eat slowly and do not eat big meals.
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- Do not eat late at night or just before bedtime.
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- Do not lie flat or bend over soon after eating.
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- Raise the head of your bed.
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- Wear loose-fitting clothing around your stomach.
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- If you are overweight, lose weight.
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- If you smoke, quit smoking.
Distributed by:
Ohm Laboratories Inc.
New Brunswick, NJ 08901
R0922
PRINCIPAL DISPLAY PANEL - 42 Capsule Bottle Carton
†Compare To
the active ingredient of
Nexium® 24HR
See new warning information
NDC 51660-027-44
Treats Frequent Heartburn
24
HR
Esomeprazole Magnesium
Delayed-Release Capsules
USP, 20 mg* / Acid Reducer
May take 1 to 4 days for full effect
ohm®
42 CAPSULES
Three 14-day courses of treatment
3 x 14 Count Bottles Inside
INGREDIENTS AND APPEARANCE
| ESOMEPRAZOLE
esomeprazole magnesium capsule, delayed release |
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| Labeler - Ohm Laboratories Inc. (184769029) |
| Registrant - Sun Pharmaceutical Industries, Inc. (146974886) |
| Establishment | |||
| Name | Address | ID/FEI | Business Operations |
|---|---|---|---|
| Ohm Laboratories Inc. | 184769029 | MANUFACTURE(51660-027) | |
| Establishment | |||
| Name | Address | ID/FEI | Business Operations |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | 918591058 | API MANUFACTURE(51660-027) | |