Product NDC: | 24451-775 |
Proprietary Name: | Lidocaine Hydrochloride |
Non Proprietary Name: | Lidocaine Hydrochloride |
Active Ingredient(s): | 20 mg/mL & nbsp; Lidocaine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24451-775 |
Labeler Name: | LLC Federal Solutions |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040014 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130624 |
Package NDC: | 24451-775-20 |
Package Description: | 100 CUP, UNIT-DOSE in 1 BOX (24451-775-20) > 20 mL in 1 CUP, UNIT-DOSE |
NDC Code | 24451-775-20 |
Proprietary Name | Lidocaine Hydrochloride |
Package Description | 100 CUP, UNIT-DOSE in 1 BOX (24451-775-20) > 20 mL in 1 CUP, UNIT-DOSE |
Product NDC | 24451-775 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lidocaine Hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20130624 |
Marketing Category Name | ANDA |
Labeler Name | LLC Federal Solutions |
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] |