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Lidocaine Hydrochloride and Dextrose
Lidocaine Hydrochloride and Dextrose - 0338-0409-02 - (Lidocaine Hydrochloride)
Drug Information of Lidocaine Hydrochloride and Dextrose
| Product NDC: | 0338-0409 |
| Proprietary Name: | Lidocaine Hydrochloride and Dextrose |
| Non Proprietary Name: | Lidocaine Hydrochloride |
| Active Ingredient(s): | 4 mg/mL & nbsp; Lidocaine Hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lidocaine Hydrochloride and Dextrose
| Product NDC: | 0338-0409 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018461 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19810422 |
Package Information of Lidocaine Hydrochloride and Dextrose
| Package NDC: | 0338-0409-02 |
| Package Description: | 250 mL in 1 BAG (0338-0409-02) |
NDC Information of Lidocaine Hydrochloride and Dextrose
| NDC Code | 0338-0409-02 |
| Proprietary Name | Lidocaine Hydrochloride and Dextrose |
| Package Description | 250 mL in 1 BAG (0338-0409-02) |
| Product NDC | 0338-0409 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lidocaine Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19810422 |
| Marketing Category Name | NDA |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | LIDOCAINE HYDROCHLORIDE |
| Strength Number | 4 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |
