Product NDC: | 55154-2354 |
Proprietary Name: | Lidocaine Hydrochloride |
Non Proprietary Name: | LIDOCAINE HYDROCHLORIDE ANHYDROUS |
Active Ingredient(s): | 40 mg/mL & nbsp; LIDOCAINE HYDROCHLORIDE ANHYDROUS |
Administration Route(s): | RETROBULBAR; TOPICAL |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-2354 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA088295 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100324 |
Package NDC: | 55154-2354-5 |
Package Description: | 5 AMPULE in 1 BAG (55154-2354-5) > 5 mL in 1 AMPULE |
NDC Code | 55154-2354-5 |
Proprietary Name | Lidocaine Hydrochloride |
Package Description | 5 AMPULE in 1 BAG (55154-2354-5) > 5 mL in 1 AMPULE |
Product NDC | 55154-2354 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | LIDOCAINE HYDROCHLORIDE ANHYDROUS |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | RETROBULBAR; TOPICAL |
Start Marketing Date | 20100324 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | LIDOCAINE HYDROCHLORIDE |
Strength Number | 40 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |