18 Amlodipine Tablet Producing, Medicine GMP

Product Details
Customization: Available
Application: Antipyretic and Anti-Inflammatory
State: Solid
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  • 18 Amlodipine Tablet Producing, Medicine GMP
  • 18 Amlodipine Tablet Producing, Medicine GMP
  • 18 Amlodipine Tablet Producing, Medicine GMP
  • 18 Amlodipine Tablet Producing, Medicine GMP
  • 18 Amlodipine Tablet Producing, Medicine GMP
  • 18 Amlodipine Tablet Producing, Medicine GMP
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Basic Info.

Model NO.
10 tablets /blister
Shape
Tablet
Type
Inorganic Chemicals
Pharmaceutical Technology
Chemical Synthesis
Drug Reg./Approval No.
300490
Drug Ad Approval No.
300490
COA
Available
Test Repot
Available
Register Dossier
Available
Period of Validity
3 Years
Transport Package
Blister
Specification
10tablets/box
Trademark
UK
Origin
UK
HS Code
2804100000
Production Capacity
5000000000000000000000PC/Year

Product Description

18 amlodipine tablet producing,medicine GMP
Amlodipine, a calcium antagonist, is used in the treatment of all types of hypertension (alone or in combination with other drugs) and angina pectoris, especially spontaneous angina (alone or in combination with other drugs). The product has a protective effect on the kidneys. Its preparations include amlodipine benzenesulfonate tablets, amlodipine mesylate tablets, and levamlodipine maleate tablets.
indications:
1. Primary hypertension. Apply alone or in combination with other anti-hypertensive drugs.

2. Chronic stable angina and variant angina. Applied alone or in combination with other anti-hypertensive drugs.

3. Coronary artery disease confirmed by angiography.
Usage and dosage:
Oral, the starting dose of 5mg once a day, and then gradually increased to 10mg per day as needed, the elderly and people with reduced renal function or the combined application of other antihypertensive drugs or anti-anginal drugs do not need to adjust the dose. However, the initial dose should be 2.5mg once daily; this dose can also be used as a therapeutic dose when other antihypertensive drugs are used.

The dose should be adjusted according to the individual response, and the general dose adjustment should be carried out in 7~14 days. If clinically necessary, dose adjustments may be initiated within a short period of time after close patient testing.



18 Amlodipine Tablet Producing, Medicine GMP

18 Amlodipine Tablet Producing, Medicine GMP18 Amlodipine Tablet Producing, Medicine GMP18 Amlodipine Tablet Producing, Medicine GMP

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