| Product NDC: | 21695-466 |
| Proprietary Name: | XYLOCAINE |
| Non Proprietary Name: | Lidocaine Hydrochloride |
| Active Ingredient(s): | 10 mg/mL & nbsp; Lidocaine Hydrochloride |
| Administration Route(s): | INFILTRATION |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 21695-466 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA006488 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19481119 |
| Package NDC: | 21695-466-20 |
| Package Description: | 20 mL in 1 VIAL, MULTI-DOSE (21695-466-20) |
| NDC Code | 21695-466-20 |
| Proprietary Name | XYLOCAINE |
| Package Description | 20 mL in 1 VIAL, MULTI-DOSE (21695-466-20) |
| Product NDC | 21695-466 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lidocaine Hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INFILTRATION |
| Start Marketing Date | 19481119 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | LIDOCAINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |