Product NDC: | 63323-490 |
Proprietary Name: | Xylocaine-MPF |
Non Proprietary Name: | LIDOCAINE HYDROCHLORIDE |
Active Ingredient(s): | 40 mg/mL & nbsp; LIDOCAINE HYDROCHLORIDE |
Administration Route(s): | RETROBULBAR; TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63323-490 |
Labeler Name: | APP Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA010417 |
Marketing Category: | NDA |
Start Marketing Date: | 20091111 |
Package NDC: | 63323-490-89 |
Package Description: | 10 AMPULE in 1 BOX (63323-490-89) > 5 mL in 1 AMPULE |
NDC Code | 63323-490-89 |
Proprietary Name | Xylocaine-MPF |
Package Description | 10 AMPULE in 1 BOX (63323-490-89) > 5 mL in 1 AMPULE |
Product NDC | 63323-490 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | LIDOCAINE HYDROCHLORIDE |
Dosage Form Name | SOLUTION |
Route Name | RETROBULBAR; TOPICAL |
Start Marketing Date | 20091111 |
Marketing Category Name | NDA |
Labeler Name | APP Pharmaceuticals, LLC |
Substance Name | LIDOCAINE HYDROCHLORIDE |
Strength Number | 40 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |