Product NDC: | 66312-461 |
Proprietary Name: | Polocaine |
Non Proprietary Name: | Mepivacaine Hydrochloride and Levonordefrin |
Active Ingredient(s): | .05; 20 mg/mL; mg/mL & nbsp; Mepivacaine Hydrochloride and Levonordefrin |
Administration Route(s): | SUBCUTANEOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66312-461 |
Labeler Name: | Dentsply Pharmaceutical |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA088388 |
Marketing Category: | NDA |
Start Marketing Date: | 19841010 |
Package NDC: | 66312-461-16 |
Package Description: | 50 CARTRIDGE in 1 CARTON (66312-461-16) > 1.7 mL in 1 CARTRIDGE |
NDC Code | 66312-461-16 |
Proprietary Name | Polocaine |
Package Description | 50 CARTRIDGE in 1 CARTON (66312-461-16) > 1.7 mL in 1 CARTRIDGE |
Product NDC | 66312-461 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Mepivacaine Hydrochloride and Levonordefrin |
Dosage Form Name | INJECTION |
Route Name | SUBCUTANEOUS |
Start Marketing Date | 19841010 |
Marketing Category Name | NDA |
Labeler Name | Dentsply Pharmaceutical |
Substance Name | LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE |
Strength Number | .05; 20 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE] |