Product NDC: | 0781-7058 |
Proprietary Name: | Lidocaine and Prilocaine |
Non Proprietary Name: | Lidocaine and Prilocaine |
Active Ingredient(s): | 25; 25 mg/g; mg/g & nbsp; Lidocaine and Prilocaine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0781-7058 |
Labeler Name: | Sandoz Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076320 |
Marketing Category: | ANDA |
Start Marketing Date: | 20030827 |
Package NDC: | 0781-7058-03 |
Package Description: | 1 TUBE in 1 CARTON (0781-7058-03) > 30 g in 1 TUBE |
NDC Code | 0781-7058-03 |
Proprietary Name | Lidocaine and Prilocaine |
Package Description | 1 TUBE in 1 CARTON (0781-7058-03) > 30 g in 1 TUBE |
Product NDC | 0781-7058 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lidocaine and Prilocaine |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20030827 |
Marketing Category Name | ANDA |
Labeler Name | Sandoz Inc. |
Substance Name | LIDOCAINE; PRILOCAINE |
Strength Number | 25; 25 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE],Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE] |