| Product NDC: | 0362-9014 |
| Proprietary Name: | Prilocaine Hydrochloride |
| Non Proprietary Name: | prilocaine hydrochloride |
| Active Ingredient(s): | 40 mg/mL & nbsp; prilocaine hydrochloride |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0362-9014 |
| Labeler Name: | Septodont Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079235 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110101 |
| Package NDC: | 0362-9014-50 |
| Package Description: | 50 CARTRIDGE in 1 CARTON (0362-9014-50) > 1.8 mL in 1 CARTRIDGE |
| NDC Code | 0362-9014-50 |
| Proprietary Name | Prilocaine Hydrochloride |
| Package Description | 50 CARTRIDGE in 1 CARTON (0362-9014-50) > 1.8 mL in 1 CARTRIDGE |
| Product NDC | 0362-9014 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | prilocaine hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20110101 |
| Marketing Category Name | ANDA |
| Labeler Name | Septodont Inc. |
| Substance Name | PRILOCAINE HYDROCHLORIDE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE] |