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] |