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Lidocaine Hydrochloride
Lidocaine Hydrochloride - 63739-457-05 - (Lidocaine Hydrochloride)
Drug Information of Lidocaine Hydrochloride
| Product NDC: | 63739-457 |
| Proprietary Name: | Lidocaine Hydrochloride |
| Non Proprietary Name: | Lidocaine Hydrochloride |
| Active Ingredient(s): | 20 mg/mL & nbsp; Lidocaine Hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lidocaine Hydrochloride
| Product NDC: | 63739-457 |
| Labeler Name: | McKesson Packaging Services Business Unit of McKesson Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040302 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100503 |
Package Information of Lidocaine Hydrochloride
| Package NDC: | 63739-457-05 |
| Package Description: | 5 POUCH in 1 BOX (63739-457-05) > 1 CARTON in 1 POUCH (63739-457-21) > 1 SYRINGE, PLASTIC in 1 CARTON > 5 mL in 1 SYRINGE, PLASTIC |
NDC Information of Lidocaine Hydrochloride
| NDC Code | 63739-457-05 |
| Proprietary Name | Lidocaine Hydrochloride |
| Package Description | 5 POUCH in 1 BOX (63739-457-05) > 1 CARTON in 1 POUCH (63739-457-21) > 1 SYRINGE, PLASTIC in 1 CARTON > 5 mL in 1 SYRINGE, PLASTIC |
| Product NDC | 63739-457 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lidocaine Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100503 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Packaging Services Business Unit of McKesson Corporation |
| 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] |
