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Mepivacaine Hydrochloride
Mepivacaine Hydrochloride - 0409-7551-01 - (Mepivacaine Hydrochloride)
Drug Information of Mepivacaine Hydrochloride
| Product NDC: | 0409-7551 |
| Proprietary Name: | Mepivacaine Hydrochloride |
| Non Proprietary Name: | Mepivacaine Hydrochloride |
| Active Ingredient(s): | 30 mg/mL & nbsp; Mepivacaine Hydrochloride |
| Administration Route(s): | DENTAL; INFILTRATION |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mepivacaine Hydrochloride
| Product NDC: | 0409-7551 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040806 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091109 |
Package Information of Mepivacaine Hydrochloride
| Package NDC: | 0409-7551-01 |
| Package Description: | 50 CARTRIDGE in 1 CARTON (0409-7551-01) > 1.8 mL in 1 CARTRIDGE |
NDC Information of Mepivacaine Hydrochloride
| NDC Code | 0409-7551-01 |
| Proprietary Name | Mepivacaine Hydrochloride |
| Package Description | 50 CARTRIDGE in 1 CARTON (0409-7551-01) > 1.8 mL in 1 CARTRIDGE |
| Product NDC | 0409-7551 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Mepivacaine Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | DENTAL; INFILTRATION |
| Start Marketing Date | 20091109 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | MEPIVACAINE HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE] |
