View drug registration information details.
Items | Registration information |
ID | 588 |
No | 588 |
Brand Name | PRELICA CAPSULE 75 MG |
Ingredients | PREGABALIN 75 MG |
Dosage Form | HARD CAPSULE |
Primary Packaging | ALU-PVC BLISTER |
Storage | STORE BELOW 30 C |
Shelf Life | 3 YEARS |
Pack Size | BLISTER PACK OF 3 X 10'S, 6 X 10'S, 10 X 10'S |
Dispensing Category | PRESCRIPTION ONLY |
ATC Classification | N03AX16 |
Pharmaceutical Class | ANTIEPILEPTICS |
Indications | FOR THE TREATMENT OF PERIPHERAL AND CENTRAL NEUROPATHIC PAIN IN ADULT, AS ADJUNCTIVE THERAPY IN ADULTS WITH PARTIAL SEIZURES WITH OR WITHOUT SECONDARY GENERALIZATION, FOR THE TREATMENT OF GENERALIZED ANXIETY DISORDER IN ADULT, FOR THE MANAGEMENT OF FIBROMYALGIA. |
Contraindications | HYPERSENSI0TVITY TO THE ACTIVE SUBSTANCE OR TO ANY OF THE EXCIPIENTS |
Side Effects | MINOR OR MODERATE INFLUENCE ON TH ABILITY TO DRIVE AND USE MACHINES, DIZZINESS AND SOMNOLENCE, NASOPHARYNGITIS, APPETITE INCREASED, EUPHORIC MOOD, CONFUSION, IRRITABILITY, VERTIGO |
Unit Price | |
EDL |
Yes |
Description | SIZE 4 CAPSULE, WITH WHITE BODY AND BROWN CAP PRINTED WITH PRE/75, CONTAINS WHITE TO OFF WHITE GRANULES |
Note | |
License Owner | DKSH LAOS COMPANY LIMITED |
Manufacturer | DUOPHARMA (M) SDN. BHD. |
Country | MALAYSIA |
Import Registration No | MAL16115039AZ |
Import Registration Date | 2016-11-25 |
Activity | CERTIFICATE RELEASED |
Applied Date | 2022-04-22 |
FDD Registration No | 06 I 5546/23 |
FDD Registration Date | 2023-06-26 |
Expiry Date | 2026-06-25 |
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