Product NDC: | 0409-7931 |
Proprietary Name: | Lidocaine Hydrochloride and Dextrose |
Non Proprietary Name: | LIDOCAINE HYDROCHLORIDE ANHYDROUS |
Active Ingredient(s): | 400 mg/100mL & nbsp; LIDOCAINE HYDROCHLORIDE ANHYDROUS |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-7931 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018388 |
Marketing Category: | NDA |
Start Marketing Date: | 20100126 |
Package NDC: | 0409-7931-32 |
Package Description: | 12 POUCH in 1 CASE (0409-7931-32) > 1 BAG in 1 POUCH > 250 mL in 1 BAG |
NDC Code | 0409-7931-32 |
Proprietary Name | Lidocaine Hydrochloride and Dextrose |
Package Description | 12 POUCH in 1 CASE (0409-7931-32) > 1 BAG in 1 POUCH > 250 mL in 1 BAG |
Product NDC | 0409-7931 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | LIDOCAINE HYDROCHLORIDE ANHYDROUS |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20100126 |
Marketing Category Name | NDA |
Labeler Name | Hospira, Inc. |
Substance Name | LIDOCAINE HYDROCHLORIDE ANHYDROUS |
Strength Number | 400 |
Strength Unit | mg/100mL |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |