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Lidocaine Hydrochloride
Lidocaine Hydrochloride - 49349-740-01 - (LIDOCAINE HYDROCHLORIDE ANHYDROUS)
Drug Information of Lidocaine Hydrochloride
| Product NDC: | 49349-740 |
| Proprietary Name: | Lidocaine Hydrochloride |
| Non Proprietary Name: | LIDOCAINE HYDROCHLORIDE ANHYDROUS |
| Active Ingredient(s): | 10 mg/mL & nbsp; LIDOCAINE HYDROCHLORIDE ANHYDROUS |
| Administration Route(s): | INFILTRATION |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lidocaine Hydrochloride
| Product NDC: | 49349-740 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088299 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130612 |
Package Information of Lidocaine Hydrochloride
| Package NDC: | 49349-740-01 |
| Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (49349-740-01) |
NDC Information of Lidocaine Hydrochloride
| NDC Code | 49349-740-01 |
| Proprietary Name | Lidocaine Hydrochloride |
| Package Description | 50 mL in 1 VIAL, MULTI-DOSE (49349-740-01) |
| Product NDC | 49349-740 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LIDOCAINE HYDROCHLORIDE ANHYDROUS |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INFILTRATION |
| Start Marketing Date | 20130612 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | LIDOCAINE HYDROCHLORIDE ANHYDROUS |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |
