Product NDC: | 68788-9799 |
Proprietary Name: | Lidocaine Hydrochloride |
Non Proprietary Name: | Lidocaine Hydrochloride |
Active Ingredient(s): | 20 mg/mL & nbsp; Lidocaine Hydrochloride |
Administration Route(s): | ORAL; TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68788-9799 |
Labeler Name: | Preferred Pharmaceuticals, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040014 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120430 |
Package NDC: | 68788-9799-1 |
Package Description: | 100 mL in 1 BOTTLE, PLASTIC (68788-9799-1) |
NDC Code | 68788-9799-1 |
Proprietary Name | Lidocaine Hydrochloride |
Package Description | 100 mL in 1 BOTTLE, PLASTIC (68788-9799-1) |
Product NDC | 68788-9799 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lidocaine Hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | ORAL; TOPICAL |
Start Marketing Date | 20120430 |
Marketing Category Name | ANDA |
Labeler Name | Preferred Pharmaceuticals, Inc |
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] |