Product NDC: | 57539-0221 |
Proprietary Name: | Lidocaine |
Non Proprietary Name: | Lidocaine |
Active Ingredient(s): | 5 g/100g & nbsp; Lidocaine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57539-0221 |
Labeler Name: | Novocol Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040911 |
Marketing Category: | ANDA |
Start Marketing Date: | 20111001 |
Package NDC: | 57539-0221-5 |
Package Description: | 1 TUBE in 1 CARTON (57539-0221-5) > 35.44 g in 1 TUBE |
NDC Code | 57539-0221-5 |
Proprietary Name | Lidocaine |
Package Description | 1 TUBE in 1 CARTON (57539-0221-5) > 35.44 g in 1 TUBE |
Product NDC | 57539-0221 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lidocaine |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20111001 |
Marketing Category Name | ANDA |
Labeler Name | Novocol Inc. |
Substance Name | LIDOCAINE |
Strength Number | 5 |
Strength Unit | g/100g |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |