View drug registration information details.
| Items | Registration information |
|---|
| ID | 653 |
|---|
| No | 653 |
|---|
| Brand Name | UTROGESTAN 200 MG |
|---|
| Ingredients | PROGESTERONE MICRONIZED PH EUR 200 MG |
|---|
| Dosage Form | SOFT CAPSULE, ORAL ROUTE |
|---|
| Primary Packaging | ALU-PVC BLISTER PACK |
|---|
| Storage | |
|---|
| Shelf Life | 36 MONTHS |
|---|
| Pack Size | BOX OF 15'S |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | DISORDERS ASSOCIATED WITH A PROGESTERONE DEFICIT IN PARTICULAR: PRE-MENSTRUAL SYNDROME, MENSTRUAL IRREGULARITIES DUE TO OVULATION DISORDERS OR ANOVULATION, BENIGN MASTOPATHY, PREMENOPAUSE, INFERTILITY CAUSED BY LUTEAL PHASE DEFECT, MENACE OF PRETERM DELIVERY |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | OVOID, SLIGHTLY YELLOW CAPSULE CONTAING A WHITISH OILY SUSPENSION |
|---|
| Note | |
|---|
| License Owner | EXAMED CO.,LTD |
|---|
| Manufacturer | CYNDEA PHARMA, S.L. |
|---|
| Country | BELGIUM |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 01 I 5170/22 |
|---|
| FDD Registration Date | 25-OCT-2024 |
|---|
| Expiry Date | 24-OCT-2029 |
|---|
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