View drug registration information details.
| Items | Registration information |
|---|
| ID | 2894 |
|---|
| No | 2894 |
|---|
| Brand Name | VALCONTIN 500 |
|---|
| Ingredients | VALPROIC ACID USP 145 MG, SODIUM VALPROATE BP 333 MG |
|---|
| Dosage Form | FILM COATED TABLET |
|---|
| Primary Packaging | ALU-ALU |
|---|
| Storage | |
|---|
| Shelf Life | 24 MONTHS |
|---|
| Pack Size | BOX OF 10 X 10'S |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | TREATMENT OF GENERALIZED SEIZURES, NOTABLY TONIC-CLONIC, ABSENCE AND MYOCLONIC SEIZURES AND ALSO FOR PARTIAL SEIZURE (SIMPLE AND COMPLEX) |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | white to off white, caplet shaped, biconvex, plain film coated tablet |
|---|
| Note | |
|---|
| License Owner | VIMPEX (LAO) CO.,LTD |
|---|
| Manufacturer | MODI-MUNDIPHARMA PRIVATE LTD |
|---|
| Country | INDIA |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 12 I 5361/22 |
|---|
| FDD Registration Date | 30-DEC-2022 |
|---|
| Expiry Date | 29-DEC-2025 |
|---|
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