View drug registration information details.
| Items | Registration information |
|---|
| ID | 876 |
|---|
| No | 876 |
|---|
| Brand Name | FEDILATE |
|---|
| Ingredients | NIFEDIPINE 20MG |
|---|
| Dosage Form | TABLETS |
|---|
| Primary Packaging | BLISTERS |
|---|
| Storage | STORE AT BELOW 25'C |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | 10 TABLETS/BLISTER, 10 BLISTER/BOX |
|---|
| Dispensing Category | PRESCRIPTION ONLY |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | ANTIHYPERTENSIVES |
|---|
| Indications | |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
Yes |
|---|
| Description | |
|---|
| Note | |
|---|
| License Owner | FACTORY NO.2 |
|---|
| Manufacturer | FACTORY No.2
|
|---|
| Country | LAO PDR |
|---|
| Import Registration No | 12 L 0800/19 |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 12 L 0800/19 |
|---|
| FDD Registration Date | 2023-04-05 |
|---|
| Expiry Date | 2026-04-04 |
|---|
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