| NDC Code | 70069-753-10 |
|---|
| Package Description | 10 VIAL in 1 CARTON (70069-753-10) / 50 mL in 1 VIAL |
|---|
| Product NDC | 70069-753 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Bupivacaine Hydrochloride |
|---|
| Non-Proprietary Name | Bupivacaine Hydrochloride |
|---|
| Dosage Form | INJECTION, SOLUTION |
|---|
| Usage | INFILTRATION; PERINEURAL |
|---|
| Start Marketing Date | 20231127 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA217792 |
|---|
| Manufacturer | Somerset Therapeutics, LLC |
|---|
| Substance Name | BUPIVACAINE HYDROCHLORIDE |
|---|
| Strength | 5 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Amide Local Anesthetic [EPC], Amides [CS], Local Anesthesia [PE] |
|---|