ID | 1217 |
No | 1217 |
Brand Name | ZOTALINE |
Ingredients | SERTRALINE HYDROCHLORIDE 55.95 MG EQ.TO SERTRALINE 50 MG |
Dosage Form | FILM-COATED TABLETS |
Primary Packaging | BLISTERPACK |
Storage | STORE BELOW 30'C, PROTECT FROM LIGHT. |
Shelf Life | 3 YEARS |
Pack Size | BOX OF 3 X10'S |
Dispensing Category | Prescription only |
ATC Classification | XX |
Pharmaceutical Class | ANTIDEPRESSANTS |
Indications | ZOTALINE IS INDICATED FOR THE TREATMENT AS FOLLOWS :
- SYMPTOMS OF DEPRESSION, INCLUDING DEPRESSION ACCOMPANIED BY SYMPTOMS OF ANXIETY, IN PATIENTS WITH OR WITHOUT A HISTORY OF MANIA. OBSESSIVE -COMPULSIVE DISORDER, PANIC DISORDER WITH OR WITHOUT AGORAPHOBIA, POST-TRAUMATIC STRESS ORDER, SOCIAL PHOBIA |
Contraindications | ZOTALINE IS CONTRAINDICATED IN PATIENTS WITH A KNOW HYPERSENSITIVITY TO SERTRALINE. CONCOMITANT USE WITH MAOI DRUG |
Side Effects | DISORDERS: ASTHENIA,CHEST PAIN, EDEMA, PERIPHERAL,FATIGUE, FEVER AND MALAISE. |
Unit Price | 10.46$ |
EDL |
No |
Description | WHITE TO OFF WHITE, CAPSULE SHAPED AND FILM COATED TABLET ENGRAVED M&H ON ONE SIDE AND ZOT AND 50 WITH SCORE - LINE ON THE OTHER SIDE. |
Note | |
License Owner | KARNYA VIENGNAKORN EXPORT-IMPORT |
Manufacturer | M & H MANUFACTURING CO., LTD |
Country | THAILAND |
Import Registration No | 1A 18/53 ( NG) |
Import Registration Date | 2010-07-23 |
Activity | CERTIFICATE RELEASED |
Applied Date | 2022-05-06 |
FDD Registration No | 03 I 3768/12 |
FDD Registration Date | 2022-09-26 |
Expiry Date | 2025-09-25 |