View drug registration information details.
| Items | Registration information |
|---|
| ID | 877 |
|---|
| No | 877 |
|---|
| Brand Name | FEDILATE |
|---|
| Ingredients | NIFEDIPINE 10MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | BLISTERPACK |
|---|
| Storage | STORE AT TEMPERATURE 15-30 C. |
|---|
| Shelf Life | 4 YEARS |
|---|
| Pack Size | 10 TABS/BLIST., 10 BLISTS/BOX |
|---|
| Dispensing Category | Prescription only |
|---|
| ATC Classification | C02DE02 |
|---|
| Pharmaceutical Class | ANTIHYPERTENSIVES |
|---|
| Indications | PROPHYLAXIS AND TREATMENT OF ANGINA AND HYPERTENTION |
|---|
| Contraindications | - |
|---|
| Side Effects | - |
|---|
| Unit Price | - |
|---|
| EDL |
Yes |
|---|
| Description | LIGHT YELLOW TABLET WITH BREAK LINE ON ONE SIDE |
|---|
| Note | |
|---|
| License Owner | FACTORY NO.2 |
|---|
| Manufacturer | FACTORY NO. 2 |
|---|
| Country | LAO PDR |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | 2011-05-26 |
|---|
| FDD Registration No | 11 L 0380/00 |
|---|
| FDD Registration Date | 2022-04-18 |
|---|
| Expiry Date | 2025-04-17 |
|---|
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