View drug registration information details.
Items | Registration information |
ID | 548 |
No | 548 |
Brand Name | METFORWAN XR 1000 |
Ingredients | METFORMIN HYDROCHLORIDE USP 1000 MG |
Dosage Form | EXTENED RELEASE TABLET |
Primary Packaging | ALU-ALU BLISTER PACK |
Storage | STORE IN A COOL, DRY, AND DARK PLACE, BELOW 30C |
Shelf Life | 3 YEARS |
Pack Size | BOX OF 10 X 10'S |
Dispensing Category | Prescription only |
ATC Classification | A10BA02 |
Pharmaceutical Class | DRUG USED IN DIABETES |
Indications | TREATMENT OF TYPE 2 DIABETES ME;;ITUS, PARTICULARLY IN OVERWEIGHT PATIENTS, WHEN DIETARY MANAGEMENT AND EXCERCISE ALONE DOES NOT RESULT IN ADEQUATE GLYCAEMIC CONTROL |
Contraindications | DIABETIC PRE-COMA, ACUTE CONDITION WITH THE POTENTIAL TO ALTER RENAL FUNCTION, ACUTE OR CHRONIC DISEASE WHICH MAY CAUSE TISSUE HYPOXIA, HEPATIC INSUFFICIENCY, ACUTE ALCOHOL INTOXICATION, ALCOHOLISM, SEVERE RENAL FAILURE |
Side Effects | NAUSEA, VOMITING, DIARRHEA, ABDOMINAL PAIN, LOSS OF APPETITE |
Unit Price | |
EDL |
Yes |
Description | WHITE TO OFF WHITE COLOR, ELONGATED, BICONVEX, UNCOATED TABLETS SCORED ON ONE SIDE |
Note | |
License Owner | DKSH LAOS COMPANY LIMITED |
Manufacturer | ARGON REMEDIES PVT.LTD |
Country | INDIA |
Import Registration No | 2/SC/P OF 1987 (FORM-28) |
Import Registration Date | 13-01-2020 |
Activity | CERTIFICATE RELEASED |
Applied Date | 2022-04-08 |
FDD Registration No | 01 I 5667/24 |
FDD Registration Date | 2024-01-26 |
Expiry Date | 2027-01-25 |
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