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NDC 41250-0712-78 heartburn relief 20 mg/1 Details
heartburn relief 20 mg/1
heartburn relief is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Meijer Distribution Inc. The primary component is FAMOTIDINE.
MedlinePlus Drug Summary
Prescription famotidine is used to treat ulcers (sores on the lining of the stomach or small intestine); gastroesophageal reflux disease (GERD, a condition in which backward flow of acid from the stomach causes heartburn and injury of the esophagus [tube that connects the mouth and stomach]); and conditions where the stomach produces too much acid, such as Zollinger-Ellison syndrome (tumors in the pancreas or small intestine that cause increased production of stomach acid). Over-the-counter famotidine is used to prevent and treat heartburn due to acid indigestion and sour stomach caused by eating or drinking certain foods or drinks. Famotidine is in a class of medications called H2 blockers. It works by decreasing the amount of acid made in the stomach.
Related Packages: 41250-0712-78Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Famotidine
Product Information
| NDC | 41250-0712 |
|---|---|
| Product ID | 41250-712_dd24164b-cd4e-4c37-92d9-2310ba0f3442 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | heartburn relief |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | famotidine |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 20 |
| Active Ingredient Units | mg/1 |
| Substance Name | FAMOTIDINE |
| Labeler Name | Meijer Distribution Inc |
| Pharmaceutical Class | Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA077351 |
| Listing Certified Through | 2024-12-31 |
Package
Package Images
NDC 41250-0712-78 (41250071278)
| NDC Package Code | 41250-712-78 |
|---|---|
| Billing NDC | 41250071278 |
| Package | 2 BOTTLE in 1 CARTON (41250-712-78) / 50 TABLET, FILM COATED in 1 BOTTLE |
| Marketing Start Date | 2022-08-11 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL 263ee489-fc3f-4578-b3a5-44f6d7757898 Details
Uses
Do not use
Ask a doctor before use if you have
- •
- had heartburn over 3 months. This may be a sign of a more serious condition.
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- heartburn with lightheadedness, sweating, or dizziness
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- 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
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- frequent wheezing, particularly with heartburn
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- unexplained weight loss
- •
- nausea or vomiting
- •
- stomach pain
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- kidney disease
Ask a doctor or pharmacist before use if you are
Stop use and ask a doctor if
Keep out of reach of children.
Directions
- •
- adults and children 12 years and over:
- •
- to relieve symptoms, swallow 1 tablet with a glass of water. Do not chew.
- •
- to prevent symptoms, swallow 1 tablet with a glass of water at any time from 10 to 60 minutesbefore eating food or drinking beverages that cause heartburn
- •
- do not use more than 2 tablets in 24 hours
- •
- children under 12 years: ask a doctor
Other information
Inactive ingredients
Package/Label Principal Display Panel
INGREDIENTS AND APPEARANCE
| HEARTBURN RELIEF
famotidine tablet, film coated |
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| Labeler - Meijer Distribution Inc (006959555) |
Revised: 8/2022
Document Id: dd24164b-cd4e-4c37-92d9-2310ba0f3442
Set id: 263ee489-fc3f-4578-b3a5-44f6d7757898
Version: 5
Effective Time: 20220811