| ID | 1989 |
|---|
| No | 1989 |
|---|
| Brand Name | TAD 600 MG/4 ML |
|---|
| Ingredients | GLUTATHIONE SODIUM SALT 646 MG EQ. TO GLUTATHIONE 600 MG/4ML |
|---|
| Dosage Form | POWDER FOR SOLUTION FOR INJECTION |
|---|
| Primary Packaging | VIAL |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | 10 POWDER VIALS + 10 SOLVENT AMPOULES 4 ML/BOX |
|---|
| Dispensing Category | |
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| ATC Classification | |
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| Pharmaceutical Class | |
|---|
| Indications | PROPHYLAXIS OF NEUROTOXICITY DUE TO CHEMOTHERAPEUTIC TREATMENT WITH CISPLATIN OR RELATED PRODUCT, FATTY DEGENERATION OF LIVER, CHRONIC HEPATITIS, TOXIC LIVER DAMAGE OF VARIOUS ETIOLGIE, INCLUDING ALCOHOL, VIRAL AND DRUGS. |
|---|
| Contraindications | |
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| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL | NULL |
|---|
| Description | WHITE HOMOGENEOUS POWDER, WITHOUT VISIBLE PARTICLES, CONTAINED IN COLORLESS GLASS VIAL |
|---|
| Note | |
|---|
| License Owner | NAKORNLUANG PHARMA EXPORT-IMPORT CO.,LTD |
|---|
| Manufacturer | BIOMEDICA FOSCAMA INDUSTRIA CHIMICO FARMACEUTICAL S.P.A. |
|---|
| Country | ITALY |
|---|
| Import Registration No | |
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| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 06 I 4515/18 |
|---|
| FDD Registration Date | 22/04/2025 |
|---|
| Expiry Date | 21/04/2030 |
|---|
