View drug registration information details.
| Items | Registration information |
|---|
| ID | 19 |
|---|
| No | 19 |
|---|
| Brand Name | DEOLIN |
|---|
| Ingredients | DROTAVERINE HYDROCHLORIDE 40 MG |
|---|
| Dosage Form | TABLET |
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| Primary Packaging | ALU-ALU |
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| Storage | |
|---|
| Shelf Life | THREE (3) YEARS |
|---|
| Pack Size | BOX OF 100 X 10'S |
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| Dispensing Category | |
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| ATC Classification | |
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| Pharmaceutical Class | |
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| Indications | FOR THE RELIEF OF SPASM OF THE SMOOTH MUSCLES IN VISCERAL ORGANS, CHOLELITHIASIS, NEPHROLITHIASIS, CHOLECYSTITIS, PYELONEPHRITIS, CYSTITIS, GASTRODUODENITIS, SPASTIC CONTIPATION, SPASM OF THE CORONARY AND PERIPHERAL ARTERIES, SPASTIC DYSMENORRHEA, SPASM OF THE SMOOTH MUSCLES DURING PARTURITION AND INSTRUMENTATION |
|---|
| Contraindications | |
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| Side Effects | |
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| Unit Price | |
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| EDL |
NULL |
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| Description | LIGHT YELLOW, ROUND, BICONVEX TABLET WITH ENGRAVED MANUFACTURER'S LOGO ON ONE SIDE AND 40 ON THE OTHER |
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| Note | |
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| License Owner | AI KEN PHARMA CO., LTD |
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| Manufacturer | UNISON LABORATORIES CO., LTD |
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| Country | THAILAND |
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| Import Registration No | |
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| Import Registration Date | |
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| Activity | CERTIFICATE RELEASED |
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| Applied Date | |
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| FDD Registration No | 03 I 3521/11 |
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| FDD Registration Date | 07-JUL-2025 |
|---|
| Expiry Date | 06-JUL-2030 |
|---|
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