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Lidocaine Hydrochloride and Dextrose
Lidocaine Hydrochloride and Dextrose - 0264-9598-20 - (LIDOCAINE HYDROCHLORIDE ANHYDROUS and DEXTROSE MONOHYDRATE)
Drug Information of Lidocaine Hydrochloride and Dextrose
| Product NDC: | 0264-9598 |
| Proprietary Name: | Lidocaine Hydrochloride and Dextrose |
| Non Proprietary Name: | LIDOCAINE HYDROCHLORIDE ANHYDROUS and DEXTROSE MONOHYDRATE |
| Active Ingredient(s): | 5; .8 g/100mL; g/100mL & nbsp; LIDOCAINE HYDROCHLORIDE ANHYDROUS and DEXTROSE MONOHYDRATE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lidocaine Hydrochloride and Dextrose
| Product NDC: | 0264-9598 |
| Labeler Name: | B. Braun Medical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019830 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19920408 |
Package Information of Lidocaine Hydrochloride and Dextrose
| Package NDC: | 0264-9598-20 |
| Package Description: | 24 CONTAINER in 1 CASE (0264-9598-20) > 250 mL in 1 CONTAINER |
NDC Information of Lidocaine Hydrochloride and Dextrose
| NDC Code | 0264-9598-20 |
| Proprietary Name | Lidocaine Hydrochloride and Dextrose |
| Package Description | 24 CONTAINER in 1 CASE (0264-9598-20) > 250 mL in 1 CONTAINER |
| Product NDC | 0264-9598 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LIDOCAINE HYDROCHLORIDE ANHYDROUS and DEXTROSE MONOHYDRATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19920408 |
| Marketing Category Name | NDA |
| Labeler Name | B. Braun Medical Inc. |
| Substance Name | DEXTROSE MONOHYDRATE; LIDOCAINE HYDROCHLORIDE ANHYDROUS |
| Strength Number | 5; .8 |
| Strength Unit | g/100mL; g/100mL |
| Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |
