View drug registration information details.
| Items | Registration information |
|---|
| ID | 593 |
|---|
| No | 593 |
|---|
| Brand Name | REVOKE - 1.5 |
|---|
| Ingredients | LEVONORGESTREL 1.50 MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | PVC-PVDC/ALU BLISTER |
|---|
| Storage | DO NOT STORE ABOVE 30 C |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | A BLISTER PACK OF 1 TABLET |
|---|
| Dispensing Category | PRESCRIPTION ONLY |
|---|
| ATC Classification | G03AD01 |
|---|
| Pharmaceutical Class | EMERGENCY CONTRACEPTIVE |
|---|
| Indications | EMERGENCY CONTRACEPTION WITHIN 72 HOURS OF UNPROTECTED SEXUAL INTERCOURSE OR FAILURE OF A CONTRACEPTIVE METHOD |
|---|
| Contraindications | HYPERSENSITIVITY TO THE ACTIVE INGREDIENT |
|---|
| Side Effects | HEADACHE, DIZIINESS, NAUSEA, ABDOMINAL PAIN, DIARRHEA, VOMITNG, FATIQUE,DYSMENORRHOEA, DELAY OF MENSES, UTERINE PAIN, BREAST, TENDERNESS |
|---|
| Unit Price | |
|---|
| EDL |
No |
|---|
| Description | ROUND, WHITE TO OFF WHITE, UNCOATED FLAT TABLET DEBOSSED "145" ON ONE SIDE AND OTHER SIDE IS PLAIN |
|---|
| Note | |
|---|
| License Owner | DKSH LAOS COMPANY LIMITED |
|---|
| Manufacturer | MYLAN LABORATORIES LIMITED |
|---|
| Country | INDIA |
|---|
| Import Registration No | G/28/1297 |
|---|
| Import Registration Date | 2016-11-04 |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | 2022-07-01 |
|---|
| FDD Registration No | 01 I 5669/24 |
|---|
| FDD Registration Date | 2024-01-26 |
|---|
| Expiry Date | 2027-01-25 |
|---|
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