View drug registration information details.
Items | Registration information |
ID | 415 |
No | 415 |
Brand Name | ALEVE 220 MG |
Ingredients | NAPROXEN SODIUM 220 MG |
Dosage Form | FILM-COATED TABLETS |
Primary Packaging | BLISTERPACK |
Storage | STORE BELOW 30C , DRY PLACE AND AWAY FROM LIGHT |
Shelf Life | 3 YEARS |
Pack Size | BOX OF 1 BLISTER X 12 TABLETS |
Dispensing Category | Over the counter |
ATC Classification | XX |
Pharmaceutical Class | ANTIRHEUMATIC, ANTI-INFLAMMATORY ANALGESICS |
Indications | RELIEF FOR THE TEMPORARY MANAGEMENT OF THE PAIN AND DISCOMFORT ASSOCIATED WITH HEADACHE, BACKACHE,MASCULAR ACHE AND PAIN, TOOTHACHE, PERIOD PAIN,MINOR PAIN OF ARTHRITIS, REDUCE FEVER SUCH AS THAT ASSOCIATED WITH THE COMMON COLD |
Contraindications | PREVIOUSLY EXHIBITED ALLERGIY TO NAPROXEN SODIUM, PATIENTS WITH A STOMACH OR INTESTINAL ULCER OR THER STOMACH DISORDERS OR WHO HAVE IMPAIRED KIDNEY FUNCTION AND HEART FAILURE |
Side Effects | ABDOMINAL DISCOMFORT, SWELLLING,STOMACH DISCOMFORT & INDIGESTION, RINGING IN THE EARS, DIZZINESS, NAUSEA,HEACHACHE |
Unit Price | XXXX |
EDL |
No |
Description | OVAL BICONVEX SHAPED LIGHT BLUE FILM-COATED TABLETS |
Note | |
License Owner | DKSH LAOS COMPANY LIMITED |
Manufacturer | BAYER BITTERFELD GMBH |
Country | GERMANY |
Import Registration No | 38457.00.00 |
Import Registration Date | 1998-06-16 |
Activity | CERTIFICATE RELEASED |
Applied Date | 2022-05-27 |
FDD Registration No | 04 I 4414/18 |
FDD Registration Date | 2022-09-14 |
Expiry Date | 2025-09-13 |
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