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Mepivacaine
Mepivacaine - 66975-416-51 - (Mepivacaine Hydrochloride and Levonordefrin)
Drug Information of Mepivacaine
| Product NDC: | 66975-416 |
| Proprietary Name: | Mepivacaine |
| 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, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mepivacaine
| Product NDC: | 66975-416 |
| Labeler Name: | Benco Dental |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088388 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110101 |
Package Information of Mepivacaine
| Package NDC: | 66975-416-51 |
| Package Description: | 5 BLISTER PACK in 1 CARTON (66975-416-51) > 10 CARTRIDGE in 1 BLISTER PACK > 1.7 mL in 1 CARTRIDGE |
NDC Information of Mepivacaine
| NDC Code | 66975-416-51 |
| Proprietary Name | Mepivacaine |
| Package Description | 5 BLISTER PACK in 1 CARTON (66975-416-51) > 10 CARTRIDGE in 1 BLISTER PACK > 1.7 mL in 1 CARTRIDGE |
| Product NDC | 66975-416 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Mepivacaine Hydrochloride and Levonordefrin |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20110101 |
| Marketing Category Name | ANDA |
| Labeler Name | Benco Dental |
| 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] |
