| NDC Code | 0703-2914-03 |
|---|
| Package Description | 10 VIAL, SINGLE-USE in 1 CARTON (0703-2914-03) / 10 mL in 1 VIAL, SINGLE-USE (0703-2914-01) |
|---|
| Product NDC | 0703-2914 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Vecuronium Bromide |
|---|
| Non-Proprietary Name | Vecuronium Bromide |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20021114 |
|---|
| End Marketing Date | 20230731 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA074688 |
|---|
| Manufacturer | Teva Parenteral Medicines, Inc. |
|---|
| Substance Name | VECURONIUM BROMIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/10mL |
|---|
| Pharmacy Classes | Neuromuscular Nondepolarizing Blockade [PE], Nondepolarizing Neuromuscular Blocker [EPC] |
|---|