View drug registration information details.
| Items | Registration information |
|---|
| ID | 390 |
|---|
| No | 390 |
|---|
| Brand Name | BFS-NICARDIPIN |
|---|
| Ingredients | NICARDIPINE HYDROCHLORIDE 10 MG/ 10 ML |
|---|
| Dosage Form | SOLUTION FOR INJECTION |
|---|
| Primary Packaging | AMPOULES |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | 10 ML/ AMPOULE, BOX OF 10, 20 ,50 AMPOULES |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
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| Pharmaceutical Class | |
|---|
| Indications | FOR THE TREATMENT OF ACUTE LIFE-THREATENING HYPERTENTION, PARTICULARLY IN THE EVENT OF: MALIGNANT ARTERIAL HYPERTENSION/HYPERTENSIVE ENCEPHALOPATHY, AORTIC DISSECTION, SEVERE PRE-ECLAMPSIA, FOR THE TREATMENT OF POST-OPERATIVE HYPERTENSION |
|---|
| Contraindications | |
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| Side Effects | |
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| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | CLEAR, COLORLESS TO PALE YELLOW |
|---|
| Note | |
|---|
| License Owner | DAOVI PHARMA IMPORT-EXPORT SOLE CO.,LTD |
|---|
| Manufacturer | HANOI CPC1 PHARMACEUTICAL JOINT STOCK COMPANY |
|---|
| Country | VIETNAM |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 10 I 5296/22 |
|---|
| FDD Registration Date | 11-NOV-2022 |
|---|
| Expiry Date | 10-NOV-2025 |
|---|
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