Product NDC: | 54569-1285 |
Proprietary Name: | Lidocaine Hydrochloride |
Non Proprietary Name: | Lidocaine Hydrochloride |
Active Ingredient(s): | 20 mg/mL & nbsp; Lidocaine Hydrochloride |
Administration Route(s): | OROPHARYNGEAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54569-1285 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040708 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070227 |
Package NDC: | 54569-1285-0 |
Package Description: | 100 mL in 1 BOTTLE (54569-1285-0) |
NDC Code | 54569-1285-0 |
Proprietary Name | Lidocaine Hydrochloride |
Package Description | 100 mL in 1 BOTTLE (54569-1285-0) |
Product NDC | 54569-1285 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lidocaine Hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | OROPHARYNGEAL |
Start Marketing Date | 20070227 |
Marketing Category Name | ANDA |
Labeler Name | A-S Medication Solutions LLC |
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] |