| Product NDC: | 17856-0775 |
| 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: | 17856-0775 |
| Labeler Name: | Atlantic Biologicals Corps |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040014 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19950710 |
| Package NDC: | 17856-0775-2 |
| Package Description: | 20 mL in 1 CUP (17856-0775-2) |
| NDC Code | 17856-0775-2 |
| Proprietary Name | Lidocaine Hydrochloride |
| Package Description | 20 mL in 1 CUP (17856-0775-2) |
| Product NDC | 17856-0775 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lidocaine Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL; TOPICAL |
| Start Marketing Date | 19950710 |
| Marketing Category Name | ANDA |
| Labeler Name | Atlantic Biologicals Corps |
| 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] |