View drug registration information details.
| Items | Registration information |
|---|
| ID | 82 |
|---|
| No | 82 |
|---|
| Brand Name | CHLORPHE 4 MG |
|---|
| Ingredients | CHLORPHENIRAMINE MALEATE 4 MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | BOTTLE |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | 1000'S /BOTTLE |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | SYMPTOMATIC RELIEF OF ALLERGY, ALLERGIC RHINITIS AND CONJUNCTIVITIS, URTICARIA, INSECT STINGS AND PRURITUS OF ALLERGIC ORIGIN, ADJUNCT IN THE EMERGENCY TREATMENT OF ANAPHYLACTIC SOCK AND SEVERE ANGIOEDEMA |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | GREEN, FLAT TABLETS WITH A BREAKLINE ON ONE SIDE |
|---|
| Note | |
|---|
| License Owner | ALPHA BEST PHARMA CO.,LTD |
|---|
| Manufacturer | ALPHA BEST PHARMA CO.,LTD |
|---|
| Country | LAO PDR |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 10 L 1217/24 |
|---|
| FDD Registration Date | 09-OCT-2024 |
|---|
| Expiry Date | 08-OCT-2029 |
|---|
Back to drug list
|
