View drug registration information details.
| Items | Registration information |
|---|
| ID | 2829 |
|---|
| No | 2829 |
|---|
| Brand Name | DIOPLUS 5/80 MG TABLET |
|---|
| Ingredients | AMLODIPINE (AS AMLODIPINE BESYLATE) 5 MG. VALSARTAN 80 MG |
|---|
| Dosage Form | FILM COATED TABLET |
|---|
| Primary Packaging | ALU-ALU BLISTER |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | BOX OF 1 X 14'S |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | TREATMENT OF ESSENTIAL HYPERTENSION, INDICATED IN ADULTS WHOSE BLOOD PRESSURE IS NOT ADEQUATELY CONTROLLED ON AMLODIPINE OR VALSARTAN MONOTHERAPY |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | GREEN, ROUND, BICONVEX FILM COATED TABLETS HAVING BOTH SIDES PLAIN |
|---|
| Note | |
|---|
| License Owner | VIMPEX (LAO) CO.,LTD |
|---|
| Manufacturer | ATCO LABORATORIES LIMITED |
|---|
| Country | PAKISTAN |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 12 I 5355/22 |
|---|
| FDD Registration Date | 30-DEC-2022 |
|---|
| Expiry Date | 29-DEC-2025 |
|---|
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