Product NDC: | 54868-2064 |
Proprietary Name: | LIDOCAINE HYDROCHLORIDE |
Non Proprietary Name: | LIDOCAINE HYDROCHLORIDE ANHYDROUS |
Active Ingredient(s): | 20 mg/mL & nbsp; LIDOCAINE HYDROCHLORIDE ANHYDROUS |
Administration Route(s): | INFILTRATION |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-2064 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA088327 |
Marketing Category: | ANDA |
Start Marketing Date: | 19940823 |
Package NDC: | 54868-2064-1 |
Package Description: | 25 VIAL, MULTI-DOSE in 1 TRAY (54868-2064-1) > 50 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 54868-2064-1 |
Proprietary Name | LIDOCAINE HYDROCHLORIDE |
Package Description | 25 VIAL, MULTI-DOSE in 1 TRAY (54868-2064-1) > 50 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 54868-2064 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | LIDOCAINE HYDROCHLORIDE ANHYDROUS |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INFILTRATION |
Start Marketing Date | 19940823 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | LIDOCAINE HYDROCHLORIDE ANHYDROUS |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |