View drug registration information details.
Items | Registration information |
ID | 1348 |
No | 1348 |
Brand Name | LINCOMYCIN 500 MG |
Ingredients | LINCOMYCIN 500 MG |
Dosage Form | CAPSULE |
Primary Packaging | BLISTERPACK |
Storage | STORE BELOW 30C, DRY PLACE, PROTECT FROM LIGHT |
Shelf Life | 2 YEARS |
Pack Size | BOX OF 10 X 10'S |
Dispensing Category | Prescription only |
ATC Classification | J01FF02 |
Pharmaceutical Class | ANTIBACTERIA |
Indications | IN THE TREATMENT OF SERIOUS INFECTIONS DUE TO SUSCEPTIBLE STRAINS OF STREPTOCOCCI, PNEUMOCOCCI AND STAPHYLOCOCCI, ITS USE SHOULD BE RESERVED FOR PENICILLIN-ALLERGIC PATIENTS OR OTHER PATIENTS FOR WHOM, IN THE JUDGMENT OF THE PHYSICIAN, A PENICILLIN IS INAPPRPRIATE |
Contraindications | IN PATIENTS PREVIOUSLY FOUND SENSITIVE TO LINCOMYCIN OR CLINDAMYCIN OR TO ANY OTHER COMPONENT OF THE PRODUCT |
Side Effects | DIARRHEA, NAUSEA, VOMITING, GLOSSITIS, STOMATITIS, ABDOMINAL PAIN, ABDOMINAL DISCOMFORT, PRURITUS |
Unit Price | |
EDL |
No |
Description | A DARK BLUE-LIGHT BLUE HARD CAPSULE, SIZE NO. 0, CONTAINING WHITE POWDER |
Note | |
License Owner | KSD PHARMA IMPORT-EXPORT CO.,LTD |
Manufacturer | NGHE AN PHARMACEUTICAL MEDICAL MATERIAL AND EQUIPMENT JOINT STOCK COMPANY (DNA PHARMA) |
Country | VIETNAM |
Import Registration No | VD-20923-14 |
Import Registration Date | 2014-12-06 |
Activity | CERTIFICATE RELEASED |
Applied Date | 2021-04-09 |
FDD Registration No | 04 I 5444/23 |
FDD Registration Date | 2023-04-11 |
Expiry Date | 2026-04-10 |
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