View drug registration information details.
| Items | Registration information |
|---|
| ID | 2017 |
|---|
| No | 2017 |
|---|
| Brand Name | TRAMADOL NC |
|---|
| Ingredients | TRAMADOL HYDROCHLORIDE USP 50 MG |
|---|
| Dosage Form | FILM COATED TABLET |
|---|
| Primary Packaging | ALU-ALU BLISTER |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | BOX OF 10 X 10'S |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | IN ADULT AND ADOLESCENTS AGED 12 YEARS AND OVER FOR THE TREATMENT AND PREVENTION OF SEVERE PAIN. |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | YELLOW COLORED, CIRCULAR SHAPED, BICONVEX FILM COATED TABLET HAVING BREAKLINE ON ONE SIDE |
|---|
| Note | |
|---|
| License Owner | NNC PHARMA CO., LTD |
|---|
| Manufacturer | ADNOVA HEALTHCARE PVT.LTD |
|---|
| Country | INDIA |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 06 I 5779/24 |
|---|
| FDD Registration Date | 27-Jun-2024 |
|---|
| Expiry Date | 26-Jun-2027 |
|---|
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