Product NDC: | 52584-282 |
Proprietary Name: | Lidocaine Hydrochloride |
Non Proprietary Name: | Lidocaine |
Active Ingredient(s): | 20 mg/mL & nbsp; Lidocaine |
Administration Route(s): | EPIDURAL; INFILTRATION |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52584-282 |
Labeler Name: | General Injectables & Vaccines |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA088294 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100401 |
Package NDC: | 52584-282-01 |
Package Description: | 1 AMPULE in 1 BAG (52584-282-01) > 2 mL in 1 AMPULE |
NDC Code | 52584-282-01 |
Proprietary Name | Lidocaine Hydrochloride |
Package Description | 1 AMPULE in 1 BAG (52584-282-01) > 2 mL in 1 AMPULE |
Product NDC | 52584-282 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lidocaine |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | EPIDURAL; INFILTRATION |
Start Marketing Date | 20100401 |
Marketing Category Name | ANDA |
Labeler Name | General Injectables & Vaccines |
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] |