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NDC 55111-0118-90 Famotidine 10 mg/1 Details
Famotidine 10 mg/1
Famotidine is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Dr.Reddys Laboratories Limited. 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: 55111-0118-90Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Famotidine
Product Information
| NDC | 55111-0118 |
|---|---|
| Product ID | 55111-118_0e165efa-c6cc-c254-e143-a757293c26b3 |
| Associated GPIs | 49200030000310 |
| GCN Sequence Number | 021688 |
| GCN Sequence Number Description | famotidine TABLET 10 MG ORAL |
| HIC3 | Z2D |
| HIC3 Description | HISTAMINE H2-RECEPTOR INHIBITORS |
| GCN | 46432 |
| HICL Sequence Number | 004521 |
| HICL Sequence Number Description | FAMOTIDINE |
| Brand/Generic | Generic |
| Proprietary Name | Famotidine |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Famotidine |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 10 |
| Active Ingredient Units | mg/1 |
| Substance Name | FAMOTIDINE |
| Labeler Name | Dr.Reddys Laboratories Limited |
| Pharmaceutical Class | Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA077367 |
| Listing Certified Through | 2024-12-31 |
Package
Package Images
NDC 55111-0118-90 (55111011890)
| NDC Package Code | 55111-118-90 |
|---|---|
| Billing NDC | 55111011890 |
| Package | 1 BOTTLE in 1 CARTON (55111-118-90) / 90 TABLET in 1 BOTTLE |
| Marketing Start Date | 2006-09-30 |
| NDC Exclude Flag | N |
| Pricing Information | |
| Price Per Unit | 0.09723 |
| Pricing Unit | EA |
| Effective Date | 2024-02-21 |
| NDC Description | FAMOTIDINE 10 MG TABLET |
| Pharmacy Type Indicator | C/I |
| OTC | Y |
| Explanation Code | 1 |
| Classification for Rate Setting | G |
| As of Date | 2024-02-21 |
This pricing file, entitled the NADAC (National Average Drug Acquisition
Cost) files, provide
state Medicaid agencies with covered outpatient drug prices by averaging
survey invoice
prices from retail community pharmacies across the United States. These
pharmacies include
independent retail community pharmacies and chain pharmacies. The prices
are updated on a
weekly and monthly basis
Standard Product Labeling (SPL)/Prescribing Information SPL 387088a6-8eaa-fc49-8050-a546d0f0fd32 Details
Uses
Warnings
Allergy alert: Do not use if you are allergic to famotidine or other acid reducers
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.
- with other acid reducers
Ask a doctor before use if you have
- 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
- kidney disease
Ask a doctor or pharmacist before use if you are taking a prescription drug. Acid reducers may interact with certain prescription drugs.
Directions
- For Famotidine 10 mg:
- 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 15 to 60 minutes before 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
- For Famotidine 20 mg:
- 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 minutes before 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
SPL UNCLASSIFIED SECTION
Tips for Managing Heartburn
- Do not lie flat or bend over after eating
- Do not wear tight-fitting clothing around the stomach
- Do not eat before bedtime
- Raise the head of your bed
- Avoid heartburn-causing foods such as rich, spicy, fatty or fried foods, chocolate, caffeine, alcohol and certain fruits and vegetables
- Eat slowly and avoid big meals
- If overweight, lose weight
- Quit smoking
INGREDIENTS AND APPEARANCE
| FAMOTIDINE
famotidine tablet |
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| FAMOTIDINE
famotidine tablet |
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| Labeler - Dr.Reddys Laboratories Limited (650562841) |
| Establishment | |||
| Name | Address | ID/FEI | Business Operations |
|---|---|---|---|
| Dr.Reddys Laboratories Limited | 918608162 | analysis(55111-118, 55111-396) , manufacture(55111-118, 55111-396) | |
| Establishment | |||
| Name | Address | ID/FEI | Business Operations |
|---|---|---|---|
| Reed Lane Inc | 001819879 | pack(55111-118, 55111-396) | |
| Establishment | |||
| Name | Address | ID/FEI | Business Operations |
|---|---|---|---|
| Dr. Reddy's Laboratories Louisiana LLC | 830397282 | analysis(55111-118, 55111-396) , manufacture(55111-118, 55111-396) | |
Revised: 8/2021
Document Id: 0e165efa-c6cc-c254-e143-a757293c26b3
Set id: 387088a6-8eaa-fc49-8050-a546d0f0fd32
Version: 11
Effective Time: 20210818