View drug registration information details.
| Items | Registration information |
|---|
| ID | 937 |
|---|
| No | 937 |
|---|
| Brand Name | ATROPINE SULFATE |
|---|
| Ingredients | ATROPINE SULFATE 0.6MG/ML |
|---|
| Dosage Form | INJECTION |
|---|
| Primary Packaging | AMPOULE |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | 10 AMP OF 1ML/BOX |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | ANTISPAMODIC |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | CLEAR & STERILE LIQUID |
|---|
| Note | |
|---|
| License Owner | FACTORY NO.2 |
|---|
| Manufacturer | FACTORY NO. 2 |
|---|
| Country | LAO PDR |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | STEP 1: RECEIVE (RENEW) |
|---|
| Applied Date | 16-MAY-2025 |
|---|
| FDD Registration No | 03 L 0051/92 |
|---|
| FDD Registration Date | 18-APR-2022 |
|---|
| Expiry Date | 17-APR-2025 |
|---|
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