View drug registration information details.
Items | Registration information |
ID | 518 |
No | 518 |
Brand Name | GLUCOPHAGE 850 MG |
Ingredients | METFORMIN HYDROCHLORIDE 850 MG EQ.TO METFORMIN BASE 662.90 MG |
Dosage Form | FILM COATED TABLET |
Primary Packaging | PVC-ALUMINIUM |
Storage | THIS MEDICAL PRODUCT DOES NOT REQUIRE ANY SPECIAL STORAGE CONDITION |
Shelf Life | 5 YEARS |
Pack Size | BOX 2 X 15'S |
Dispensing Category | Prescription only |
ATC Classification | A01BA02 |
Pharmaceutical Class | ANTIDIABETE |
Indications | TREATMENT OF TYPE 2 DIABETES IN ADULT, PARTICULARLY IN OVERWEIGHT PATIENTS, WHEN DIETARY MANAGEMENT AND EXCERCISE ALONE DOES NOT RESULT IN ADEQUATE GLYCAEMIC CONTROL |
Contraindications | HYPERSENSITIVITY, DIABETIC KETOACIDOSIS, DIABETIC PRE-COMA, MODERATE AND SEVERE RENAL FAILURE DYSFUNCTION, HEPATIC INSUFFICIENCY, ACUTE ALCOHOL INTOXICATION, ALCOHOLISM, SEVERE INFECTION, SHOCK |
Side Effects | TASTE DISTURBANCE, GI DISORDER SUCH AS NAUSEA, VOMITTING, DIARRHEA, ABDOMINAL PAIN AND LOSS OF APPETITE, PRURITUS, URTICARIA, MACULOPAPULAR RASH |
Unit Price | |
EDL |
Yes |
Description | WHITE, CIRCULAR, CONVEX, FILM COATED TABLET |
Note | |
License Owner | DKSH LAOS COMPANY LIMITED |
Manufacturer | MERCK SANTE S.A.S |
Country | FRANCE |
Import Registration No | 304 480 -2 |
Import Registration Date | 21.03.1996 |
Activity | CERTIFICATE RELEASED |
Applied Date | 2024-02-14 |
FDD Registration No | 02 I 5046/21 |
FDD Registration Date | 2024-06-22 |
Expiry Date | 2027-06-21 |
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