| 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: | 0781-7058-05 |
| Package Description: | 5 TUBE in 1 CARTON (0781-7058-05) > 5 g in 1 TUBE |
| NDC Code | 0781-7058-05 |
| Proprietary Name | Lidocaine and Prilocaine |
| Package Description | 5 TUBE in 1 CARTON (0781-7058-05) > 5 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] |