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Lidocaine
Lidocaine - 63323-202-02 - (LIDOCAINE HYDROCHLORIDE)
Drug Information of Lidocaine
| Product NDC: | 63323-202 |
| Proprietary Name: | Lidocaine |
| Non Proprietary Name: | LIDOCAINE HYDROCHLORIDE |
| Active Ingredient(s): | 20 mg/mL & nbsp; LIDOCAINE HYDROCHLORIDE |
| Administration Route(s): | INFILTRATION; PERINEURAL |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lidocaine
| Product NDC: | 63323-202 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080404 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100527 |
Package Information of Lidocaine
| Package NDC: | 63323-202-02 |
| Package Description: | 25 VIAL in 1 TRAY (63323-202-02) > 2 mL in 1 VIAL |
NDC Information of Lidocaine
| NDC Code | 63323-202-02 |
| Proprietary Name | Lidocaine |
| Package Description | 25 VIAL in 1 TRAY (63323-202-02) > 2 mL in 1 VIAL |
| Product NDC | 63323-202 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LIDOCAINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INFILTRATION; PERINEURAL |
| Start Marketing Date | 20100527 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, 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] |
