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NDC 70518-0274-01 AMLODIPINE BESYLATE 5 mg/1 Details

AMLODIPINE BESYLATE 5 mg/1

AMLODIPINE BESYLATE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is AMLODIPINE BESYLATE.

MedlinePlus Drug Summary

Amlodipine is used alone or in combination with other medications to treat high blood pressure in adults and children 6 years and older. It is also used to treat certain types of angina (chest pain) and coronary artery disease (narrowing of the blood vessels that supply blood to the heart). Amlodipine is in a class of medications called calcium channel blockers. It lowers blood pressure by relaxing the blood vessels so the heart does not have to pump as hard. It controls chest pain by increasing the supply of blood to the heart. If taken regularly, amlodipine controls chest pain, but it does not stop chest pain once it starts. Your doctor may prescribe a different medication to take when you have chest pain. High blood pressure is a common condition and when not treated, can cause damage to the brain, heart, blood vessels, kidneys and other parts of the body. Damage to these organs may cause heart disease, a heart attack, heart failure, stroke, kidney failure, loss of vision, and other problems. In addition to taking medication, making lifestyle changes will also help to control your blood pressure. These changes include eating a diet that is low in fat and salt, maintaining a healthy weight, exercising at least 30 minutes most days, not smoking, and using alcohol in moderation.

Related Packages: 70518-0274-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Amlodipine

Product Information

NDC	70518-0274
Product ID	70518-0274_0e2424f4-0013-42b0-e063-6394a90a780d
Associated GPIs	34000003100330
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	AMLODIPINE BESYLATE
Proprietary Name Suffix	n/a
Non-Proprietary Name	AMLODIPINE BESYLATE
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	5
Active Ingredient Units	mg/1
Substance Name	AMLODIPINE BESYLATE
Labeler Name	REMEDYREPACK INC.
Pharmaceutical Class	Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA077073
Listing Certified Through	2025-12-31

Package

NDC 70518-0274-01 (70518027401)

Pricing Information	N/A
NDC Package Code	70518-0274-1
Billing NDC	70518027401
Package	30 TABLET in 1 BLISTER PACK (70518-0274-1)
Marketing Start Date	2017-03-16
NDC Exclude Flag	N