View drug registration information details.
| Items | Registration information |
|---|
| ID | 362 |
|---|
| No | 362 |
|---|
| Brand Name | AMPICIN |
|---|
| Ingredients | AMPICILLIN SODIUM EQ.TO AMPICILLIN 1G |
|---|
| Dosage Form | POWDER FOR SOLUTION FOR INJECTION |
|---|
| Primary Packaging | VIAL |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | BOX OF 10 VIALS |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | TREATMENT OF INFECTIONS CAUSED BY SUSCEPTIBLE STRAINS OF THE DESIGNATED ORGANISMS IN THE FOLLOWING CONDITIONS: RESPIRATORY TRACT INFECTIONS CAUSED BY S. PNEUMONIA ,BACTERIAL MENINGITIS, SEPTICEMIA AND ENDOCARDITIS, URINARY TRACT INFECTION, GASTRO INTESTINAL INFECTIONS |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | WHITE OR ALMOST WHITE POWDER OR CRYSTALLINE POWDER |
|---|
| Note | |
|---|
| License Owner | CBF PHARMA CO.,LTD |
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| Manufacturer | NORTH CHINA PHARMACEUTICAL CO., LTD |
|---|
| Country | CHINA |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 11 I 3923/13 |
|---|
| FDD Registration Date | 26-SEP-2022 |
|---|
| Expiry Date | 25-SEP-2025 |
|---|
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