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Amlodipine-Benazepril 10-40 Mg Cap 100

  • Manufacturer Name : Dr Reddys Laboratories
  • MFG # : 55111058601
  • NDC : 55111058601
  • Distributor Name : AmeriSource Bergen
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Product Properties:

Description -
Description N
DESI Drug Ind $0.24; 04/01/2017
DESI Drug Ind -
DESI2 Drug Ind -
Drug Category N
Drug Category USES: This product is a combination of two drugs: a calcium channel blocker (amlodipine) and an ACE inhibitor (benazepril). It is used to treat high blood pressure. It works by relaxing blood vessels so that blood can flow more easily. Lowering high blood pressure helps prevent strokes, heart attacks and kidney problems.
Drug Type Code 1
Drug Type Code COMMON BRAND NAME(S): Lotrel
FDA Approval Date 07/05/2011
FDA Therap Equiv AB
HCPCS -
HCPCS 1
Market Entry Date 07/05/2011
Medical Coverage -
Medical Coverage -
Termination Date (am-LOE-di-peen/ben-AZ-e-pril)
Termination Date -
Unit CAP
Units Per Pkg 1
Active Ingredients 3598 benazepril HCl 86541744; 3673 amlodipine besylate 111470996
Active Ingredients 3598 benazepril HCl 86541744; 3673 amlodipine besylate 111470996
AHFS Class 24280800 DIHYDROPYRIDINES; 24081208 DIHYDROPYRIDINES (ANTIHYPERTENSIVE); 24280000 CALCIUM-CHANNEL BLOCKING AGENTS; 24320400 ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; 24084404 ANGIOTENSIN-CONVERT.ENZYME INHIB(HYPOTN); 24129200 VASODILATING AGENTS, MISCELLANEOUS; 24089200 HYPOTENSIVE AGENTS, MISCELLANEOUS
AHFS Class 24280800 DIHYDROPYRIDINES; 24081208 DIHYDROPYRIDINES (ANTIHYPERTENSIVE); 24280000 CALCIUM-CHANNEL BLOCKING AGENTS; 24320400 ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; 24084404 ANGIOTENSIN-CONVERT.ENZYME INHIB(HYPOTN); 24129200 VASODILATING AGENTS, MISCELLANEOUS; 24089200 HYPOTENSIVE AGENTS, MISCELLANEOUS
DEA Class NC
DEA Class NC
Dose Form CAPSULE
Dose Form CAPSULE
Fine Line Class 850085008510 All Rx Products
Fine Line Class 850085008510 All Rx Products
Gen Code and Des 60723 amlodipine besylate/benazepril ORAL CAPSULE 10 MG-40MG
Gen Code and Des 60723 amlodipine besylate/benazepril ORAL CAPSULE 10 MG-40MG
Inactive Ingredients 10141 red dye; 10143 yellow dye; 2432 lactose 64044515; 2537 povidone 9003398; 2549 gelatin 9000708; 9290 cremophor el (polyethoxlated castor oil)
Inactive Ingredients 10141 red dye; 10143 yellow dye; 2432 lactose 64044515; 2537 povidone 9003398; 2549 gelatin 9000708; 9290 cremophor el (polyethoxlated castor oil)
OMP Family -
OMP Family -
Product Category RX Pharmaceuticals
Product Category RX Pharmaceuticals
Strength 10-40 MG
Strength 10-40 MG
Common Brand Name -
Common Brand Name COMMON BRAND NAME(S): Lotrel
Drug Interaction DRUG INTERACTIONS: See also Precautions section. Drug interactions may change how your medications work or increase your risk for serious side effects. This document does not contain all possible drug interactions. Keep a list of all the products you use (including prescription/nonprescription drugs and herbal products) and share it with your doctor and pharmacist. Do not start, stop, or change the dosage of any medicines without your doctor's approval. Some products that may interact with this drug include: aliskiren, certain drugs that weaken the immune system/increase the risk of infection (such as everolimus, sirolimus), lithium, drugs that may increase the level of potassium in the blood (such as ARBs including losartan/valsartan, birth control pills containing drospirenone), gold injections, sacubitril. Some products have ingredients that could raise your blood pressure. Tell your pharmacist what products you are using, and ask how to use them safely (especially cough-and-cold products, diet aids, or NSAIDs such as ibuprofen/naproxen). A very serious reaction may occur if you are getting injections for bee/wasp sting allergy (desensitization) and are also taking benazepril. Make sure all your doctors know which medicines you are using.
Drug Interaction -
Allocation Period -
Allocation Period -
Case Quantity 24
Case Quantity 24
Drug Form Pack Size 100
Drug Form Pack Size 100
Form CAPSULES
Form CAPSULES
Hazard Code -
Hazard Code -
Listed Chemical -
Listed Chemical -
NIOSH Code -
NIOSH Code -
Orange Book AB Products meeting necessary bioequivalence requirements.
Orange Book AB Products meeting necessary bioequivalence requirements.
Retail Pack Quantity 1
Retail Pack Quantity 1
Returnable Status Returnable
Returnable Status Returnable
Special Storage Cond 00 None
Special Storage Cond 00 None
Temp Zone 10 Room Temperature
Temp Zone 10 Room Temperature
Unit EA
Unit EA
Unit Size 100
Unit Size 100
How to Use HOW TO USE: Read the Patient Information Leaflet if available from your pharmacist before you start taking this medicine. If you have any questions, ask your doctor or pharmacist. Take this medication by mouth with or without food as directed by your doctor, usually once daily. The dosage is based on your medical condition and response to treatment. Use this medication regularly in order to get the most benefit from it. To help you remember, take it at the same time each day. Keep taking this medication even if you feel well. Most people with high blood pressure do not feel sick. It may take 1 to 2 weeks before you get the full benefit of this medication. Tell your doctor if your condition does not get better or if it gets worse (your blood pressure readings remain high or increase).
How to Use -
Missed Dose 1
Missed Dose MISSED DOSE: If you miss a dose, take it as soon as you remember. If it is near the time of the next dose, skip the missed dose. Take your next dose at the regular time. Do not double the dose to catch up.
Notes NOTES: Do not share this medication with others. Lifestyle changes that may help this medication work better include exercising, stopping smoking, and eating a low-cholesterol/low-fat diet. Consult your doctor for more details. Lab and/or medical tests (such as kidney function, potassium levels) should be done while you are taking this medication. Keep all medical and lab appointments. Consult your doctor for more details. Check your blood pressure and pulse (heart rate) regularly while taking this medication. Learn how to check your own blood pressure and pulse at home, and share the results with your doctor.
Notes CAP
Overdose AB
Overdose OVERDOSE: If someone has overdosed and has serious symptoms such as passing out or trouble breathing, call 911. Otherwise, call a poison control center right away. US residents can call their local poison control center at 1-800-222-1222. Canada residents can call a provincial poison control center. Symptoms of overdose may include: severe dizziness, fainting, and unusually fast or slow heartbeat.
Phonetic Pronunciation (am-LOE-di-peen/ben-AZ-e-pril)
Phonetic Pronunciation -
Precautions -
Precautions PRECAUTIONS: Before taking this medication, tell your doctor or pharmacist if you are allergic to amlodipine or benazepril; or to other dihydropyridine calcium channel blockers (such as nisoldipine, nifedipine); or to other ACE inhibitors (such as captopril, lisinopril); or if you have any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details. Before using this medication, tell your doctor or pharmacist your medical history, especially of: history of an allergic reaction which included swelling of the face/lips/tongue/throat (angioedema), blood filtering procedures (such as LDL apheresis, dialysis), liver disease, a certain structural heart problem (aortic stenosis). This drug may make you dizzy. Alcohol or marijuana (cannabis) can make you more dizzy. Do not drive, use machinery, or do anything that needs alertness until you can do it safely. Limit alcoholic beverages. Talk to your doctor if you are using marijuana (cannabis). Too much sweating, diarrhea, or vomiting may cause dehydration and increase your risk of lightheadedness. Report prolonged diarrhea or vomiting to your doctor. Be sure to drink enough fluids to prevent dehydration unless your doctor directs you otherwise. Before having surgery, tell your doctor or dentist about all the products you use (including prescription drugs, nonprescription drugs, and herbal products). This product may increase your potassium levels. Before using potassium supplements or salt substitutes that contain potassium, consult your doctor or pharmacist. Older adults may be more sensitive to the side effects of this drug, including dizziness, increases in potassium level, and change in the amount of urine (kidney problems). Tell your doctor if you are pregnant or plan to become pregnant. You should not become pregnant while using this medication. Benazepril may harm an unborn baby. If you become pregnant, talk to your doctor right away about the risks and benefits of this medication. See also Warning section. This product passes into breast milk. Consult your doctor before breast-feeding.
Side Effects SIDE EFFECTS: Dizziness or light-headedness may occur as your body adjusts to the medication. Dry cough or swelling hands/ankles/feet may also occur. If any of these effects last or get worse, tell your doctor or pharmacist promptly. To reduce the risk of dizziness and lightheadedness, get up slowly when rising from a sitting or lying position. Remember that this medication has been prescribed because your doctor has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects. Tell your doctor right away if any of these serious side effects occur: fainting, fast/irregular/pounding heartbeat, symptoms of a high potassium blood level (such as muscle weakness, slow/irregular heartbeat), signs of kidney problems (such as change in the amount of urine). This product may rarely cause serious (possibly fatal) liver disease. Get medical help right away if you have any symptoms of liver damage, including: nausea/vomiting that doesn't stop, loss of appetite, stomach/abdominal pain, yellowing eyes/skin, dark urine. Some people who already have severe heart disease may rarely develop worsening chest pain or a heart attack after starting this medication or increasing the dose. Get medical help right away if you experience: worsening chest pain, symptoms of a heart attack (such as chest/jaw/left arm pain, shortness of breath, unusual sweating). A very serious allergic reaction to this drug is rare. However, get medical help right away if you notice any symptoms of a serious allergic reaction, including: rash, itching/swelling (especially of the face/tongue/throat), severe dizziness, trouble breathing. This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist. In the US - Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 or at www.fda.gov/medwatch. In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.
Side Effects -
Storage 07/05/2011
Storage STORAGE: Store at room temperature away from light and moisture. Do not store in the bathroom. Keep all medications away from children and pets. Do not flush medications down the toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is expired or no longer needed. Consult your pharmacist or local waste disposal company.
Uses USES: This product is a combination of two drugs: a calcium channel blocker (amlodipine) and an ACE inhibitor (benazepril). It is used to treat high blood pressure. It works by relaxing blood vessels so that blood can flow more easily. Lowering high blood pressure helps prevent strokes, heart attacks and kidney problems.
Uses -

Frequently Asked Questions(FAQs)

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Amlodipine-Benazepril 10-40 Mg Cap 100 is manufactured by Dr Reddys Laboratories.
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