View drug registration information details.
| Items | Registration information |
|---|
| ID | 2853 |
|---|
| No | 2853 |
|---|
| Brand Name | MAXRON 0.4 MG |
|---|
| Ingredients | TAMSULOSIN HYDROCHLORIDE EQ.TO TAMSULOSIN 0.4 MG |
|---|
| Dosage Form | CAPSULE |
|---|
| Primary Packaging | ALU-ALU BLISTERPACK |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | 2 X 5'S/BOX |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | TREATMENT OF MODERATE TO SEVERE SYMPTOMS OF BENIGN PROSTATIC HYPERPLASIA(BPH), REDUCTION IN THE RISK OF ACUTE URINARY RETENTION AND SURGERY IN PATIENTS WITH MODERATE TO SEVERE SYMPTOM OF BPH. |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | WHITE PELLETS FILLED IN CAPSULE SHELL WITH TRANSPARENT BODY AND REDDISH BROWN CAP |
|---|
| Note | |
|---|
| License Owner | VIMPEX (LAO) CO.,LTD |
|---|
| Manufacturer | WILSHIRE LABORATORIES(PVT) LTD |
|---|
| Country | PAKISTAN |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 11 I 4623/18 |
|---|
| FDD Registration Date | 26-SEP-2022 |
|---|
| Expiry Date | 25-SEP-2025 |
|---|
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