| NDC Code | 47335-931-44 |
|---|
| Package Description | 10 VIAL in 1 BOX (47335-931-44) / 10 mL in 1 VIAL (47335-931-40) |
|---|
| Product NDC | 47335-931 |
|---|
| 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 | 20141215 |
|---|
| End Marketing Date | 20270331 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA079001 |
|---|
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|
| Substance Name | VECURONIUM BROMIDE |
|---|
| Strength | 1 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Neuromuscular Nondepolarizing Blockade [PE], Nondepolarizing Neuromuscular Blocker [EPC] |
|---|