View drug registration information details.
Items | Registration information |
ID | 547 |
No | 547 |
Brand Name | METFORMIN 1000 MG |
Ingredients | METFORMIN HYDROCHLORIDE 1000 MG |
Dosage Form | FILM COATED TABLET |
Primary Packaging | PVC/ALU BLISTER |
Storage | STORE BELOW 30 C |
Shelf Life | 3 YEARS |
Pack Size | BOX OF 60 TABLETS |
Dispensing Category | PRESCRIPTION ONLY |
ATC Classification | A10BA02 |
Pharmaceutical Class | ANTIDIABET |
Indications | TREATMENT OF TYPE 2 DIABETES MELLITUS, PARTICULARLY IN OVERWEIGHT PATIENTS WHEN DIETARY MANAGEMENT AND EXCERCISE ALONE DOES NOT RESULT IN ADEQUATE GLYCAEMIC CONTROL |
Contraindications | HYPERSENSITIVITY, DIABETIC PRE-COMA, SEVERE RENAL FAILURE, ACUTE CONDITIONS WITH POTENTIAL TO ALTER RENAL FUNCTION, HEPATIC INSUFFICIENCY |
Side Effects | NAUSEA, VOMITING, DIARRHEA, abdominal pain, loss of appetite |
Unit Price | |
EDL |
Yes |
Description | WHITE, OVAL, BICONVEX FILM COATED TABLET, SCORED, MARKED " M1G" ON ONE SIDE AND PLAIN ON THE REVERSE SIDE |
Note | |
License Owner | DKSH LAOS COMPANY LIMITED |
Manufacturer | LEK S.A |
Country | AUSTRIA |
Import Registration No | 1-26266 |
Import Registration Date | 2006-03-23 |
Activity | CERTIFICATE RELEASED |
Applied Date | 2020-12-03 |
FDD Registration No | 07 I 5257/22 |
FDD Registration Date | 2022-08-17 |
Expiry Date | 2025-08-16 |
Back to drug list
|