Product NDC: | 76478-479 |
Proprietary Name: | Xylocaine |
Non Proprietary Name: | Lidocaine Hydrochloride |
Active Ingredient(s): | .5 mg/18mL & nbsp; Lidocaine Hydrochloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | JELLY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76478-479 |
Labeler Name: | Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.) |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA008816 |
Marketing Category: | NDA |
Start Marketing Date: | 20120701 |
Package NDC: | 76478-479-05 |
Package Description: | 1 TUBE in 1 CARTON (76478-479-05) > 5 mL in 1 TUBE |
NDC Code | 76478-479-05 |
Proprietary Name | Xylocaine |
Package Description | 1 TUBE in 1 CARTON (76478-479-05) > 5 mL in 1 TUBE |
Product NDC | 76478-479 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lidocaine Hydrochloride |
Dosage Form Name | JELLY |
Route Name | TOPICAL |
Start Marketing Date | 20120701 |
Marketing Category Name | NDA |
Labeler Name | Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.) |
Substance Name | LIDOCAINE HYDROCHLORIDE |
Strength Number | .5 |
Strength Unit | mg/18mL |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |