View drug registration information details.
Items | Registration information |
ID | 1367 |
No | 1367 |
Brand Name | MYVITA CALCIUM 500 |
Ingredients | CALCIUM LACTATE GLUCONATE 2 940 MG, CALCIUM CARBONATE 300 MG |
Dosage Form | EFFERVESCENT TABLET |
Primary Packaging | TUBE |
Storage | STORE IN DRY PLACE, AT TEMPERATURE BELOW 30 C AND AVOID SUNLIGHT |
Shelf Life | 2 YEARS |
Pack Size | BOX OF 20'S/TUBE |
Dispensing Category | - |
ATC Classification | - |
Pharmaceutical Class | MINERALS SUPPLEMENT |
Indications | OSTEOPOROSIS OF VARIOUS ORIGINS: MENOPAUSE, ELDER, GASTRECTOMY, PREVENTION OF PRE AND POSTMENOPAUSAL BONE DEMINERALIZATION, INCREASED DEMAND FOR CALCIUM IN PREGNANT AND LACTATING WOMAN, IN GROWING CHILDREN, RICKETS AND OSTEOMALACIA, TREATMENT OF SEIZURE |
Contraindications | HYPERSENSITIVITY, HYPERCALCAEMIA, HYPERCALCIUREA, CALCIUM LITHIASIS, TISSUE CALCIFICATION, SEVERE RENAL FAILURE |
Side Effects | EXCESSIVE CALCIUM LEVEL IN BLOOD, EXCESSIVE EXCRETION OF CALCIUM IN THE URINE |
Unit Price | |
EDL |
No |
Description | WHITE-CIRCULAR EFFERVESCENT TABLETS MAKE A SLIGHTLY OPAQUE SOLUTION WHEN DISSOLVING IN WATER, TABLET IS DRY AND INTACT |
Note | |
License Owner | KSD PHARMA IMPORT-EXPORT CO.,LTD |
Manufacturer | S.P.M CORPORATION |
Country | VIETNAM |
Import Registration No | VD-21971-14 |
Import Registration Date | 2014-12-08 |
Activity | CERTIFICATE RELEASED |
Applied Date | 2022-09-16 |
FDD Registration No | 11 I 4841/19 |
FDD Registration Date | 2023-04-19 |
Expiry Date | 2026-04-18 |
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