Product NDC: | 55154-3189 |
Proprietary Name: | Lidocaine Hydrochloride |
Non Proprietary Name: | LIDOCAINE HYDROCHLORIDE |
Active Ingredient(s): | 20 mg/mL & nbsp; LIDOCAINE HYDROCHLORIDE |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-3189 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040302 |
Marketing Category: | ANDA |
Start Marketing Date: | 20101129 |
Package NDC: | 55154-3189-8 |
Package Description: | 1 SYRINGE, PLASTIC in 1 BAG (55154-3189-8) > 5 mL in 1 SYRINGE, PLASTIC |
NDC Code | 55154-3189-8 |
Proprietary Name | Lidocaine Hydrochloride |
Package Description | 1 SYRINGE, PLASTIC in 1 BAG (55154-3189-8) > 5 mL in 1 SYRINGE, PLASTIC |
Product NDC | 55154-3189 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | LIDOCAINE HYDROCHLORIDE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20101129 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | LIDOCAINE HYDROCHLORIDE |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |