Antiallergic Loratadine Tablets 5mg and 10mg with GMP Certification

Product Details
Customization: Available
Application: Internal Medicine
Usage Mode: For oral administration
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  • Antiallergic Loratadine Tablets 5mg and 10mg with GMP Certification
  • Antiallergic Loratadine Tablets 5mg and 10mg with GMP Certification
  • Antiallergic Loratadine Tablets 5mg and 10mg with GMP Certification
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Basic Info.

Model NO.
AMC12116
State
Solid
Shape
Tablet
Type
Organic Chemicals
Pharmaceutical Technology
Chemical Synthesis
Deliver Time
30~60 Days
Standard Available
Bp, Cp
OEM/ODM
Support
Transport Package
10*10/Box
Specification
5mg 10mg
Trademark
Medipharm, Shinepharm, OEM
Origin
China
HS Code
3004909099
Production Capacity
1000000 Boxes/Month

Product Description

Antiallergic Loratadine Tablets 5mg and 10mg with GMP Certification
 
Characteristics:
This product is white or quasi-white.
Indications:
To relieve symptoms associated with allergic rhinitis, such as sneezing, runny nose, itchy nose, stuffy nose, and itching and burning of the eyes. Nasal and ocular signs and symptoms are quickly relieved after oral administration. It is also applicable to relieve the symptoms and signs of chronic urticaria, pruritus and other allergic skin diseases.
Usage And Dosage:

Oral.
Adults and children 12 years and older: 1 tablet (10 mg), once daily.
Children aged 2 to 12:
Weight >30 kg: 1 tablet (10 mg), once a day.
Weight ≤30 kg: one half tablet (5 mg), once a day.
 
Notes:
1. Patients with severe liver insufficiency should use it under the guidance of a doctor.
2. Use with caution during pregnancy and lactation.
3. Use should be discontinued approximately 48 hours before the skin test as antihistamines can prevent or reduce the occurrence of positive reactions.
4.People who are allergic to this product should not use it.
5. Do not use this product when its character changes.
6. Keep out of reach of children.
7. Children must be used under adult supervision.
8. If you are using other medicines, consult your doctor or pharmacist before using this product.
9.The safety and efficacy of this product in children under 9.6 years old have not been determined, please consult your physician or pharmacist.
10. For patients with liver and kidney dysfunction, the dosage should be reduced to 10 mg once every 2 days or under the guidance of a doctor.
11. Because the plasma concentration of elderly patients is higher than that of healthy people, the occurrence of adverse reactions in elderly patients should be paid close attention to when using this product for a long time.
12. Drowsiness, arrhythmia, and headache may occur in adults who take excessive doses (40-180 mg). Once the above symptoms occur, immediately give symptomatic and supportive treatment. Treatment includes emesis followed by activated carbon adsorption of unabsorbed drugs. If emesis is not successful, gastric lavage with normal saline is performed to dilute the drug concentration in the intestinal tract. Loratadine cannot be removed by hemodialysis, and it is not clear whether peritoneal dialysis can remove this product.
  
Interactions:
1. Simultaneous use of ketoconazole, macrolide antibiotics, cimetidine, theophylline and other drugs will increase the plasma concentration of loratadine, should be used with caution. Other drugs known to inhibit liver metabolism should be used with caution until they interact with loratadine.
2. Drug interactions may occur if used in conjunction with other medications. Consult your physician or pharmacist for details.


Storage:
seal preservation

Antiallergic Loratadine Tablets 5mg and 10mg with GMP CertificationAntiallergic Loratadine Tablets 5mg and 10mg with GMP CertificationAntiallergic Loratadine Tablets 5mg and 10mg with GMP CertificationAntiallergic Loratadine Tablets 5mg and 10mg with GMP CertificationAntiallergic Loratadine Tablets 5mg and 10mg with GMP CertificationAntiallergic Loratadine Tablets 5mg and 10mg with GMP Certification

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