View drug registration information details.
| Items | Registration information |
|---|
| ID | 557 |
|---|
| No | 557 |
|---|
| Brand Name | PRELICA CAPSULE 150 MG |
|---|
| Ingredients | PREGABALIN 150 MG |
|---|
| Dosage Form | HARD CAPSULE |
|---|
| Primary Packaging | ALU-PVC BLISTER |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | BLISTER PACK OF 3 X 10'S, 6 X 10'S, 10 X 10'S |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | FOR THE TREATMENT OF PERIPHERAL AND CENTRAL NEUROPATHIC PAIN IN ADULT, AS ADNUNCTIVE THERAPY IN ADULTS WITH PARTIAL SEIZURES WITH OT WITHOUT SECONDARY GENERALIZATION, FOR THE TREATMENT OF GENERALIZED ANXIETY DISORDER IN ADULT, FOR THE MANAGEMENT OF FIBROMYALGIA |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | SIZE 2 CAPSULE, WITH OPAQUE WHITE BODY AND CAP PRINTED WITH PRE/150, CONTAINS WHITE TO OFF WHITE GRANULES |
|---|
| Note | |
|---|
| License Owner | DKSH LAOS COMPANY LIMITED |
|---|
| Manufacturer | DUOPHARMA (M) SDN BHD. |
|---|
| Country | MALAYSIA |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 06 I 5545/23 |
|---|
| FDD Registration Date | 26-Jun-2023 |
|---|
| Expiry Date | 25-Jun-2026 |
|---|
Back to drug list
|
