View drug registration information details.
| Items | Registration information |
|---|
| ID | 951 |
|---|
| No | 951 |
|---|
| Brand Name | NORFLOXACIN |
|---|
| Ingredients | NORFLOXACIN 400 MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | BLISTERPACK |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | 10 TABLETS/BLISTER |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | INFECTIONS CAUSED BY SENSITIVE PATHOGENS : GONORRHEA, PNEUMONIA |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | W2HITE TABLETS. ON ONE SIDE HAVE NO.2 |
|---|
| Note | |
|---|
| License Owner | FACTORY NO.2 |
|---|
| Manufacturer | FACTORY NO. 2 |
|---|
| Country | LAO PDR |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 01 L 0675/16 |
|---|
| FDD Registration Date | 11-SEP-2023 |
|---|
| Expiry Date | 10-SEP-2026 |
|---|
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