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curacaine
curacaine - 51350-010-01 - (Lidocaine)
Drug Information of curacaine
| Product NDC: | 51350-010 |
| Proprietary Name: | curacaine |
| Non Proprietary Name: | Lidocaine |
| Active Ingredient(s): | 40 mg/mL & nbsp; Lidocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of curacaine
| Product NDC: | 51350-010 |
| Labeler Name: | Transdermal Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120912 |
Package Information of curacaine
| Package NDC: | 51350-010-01 |
| Package Description: | 30 mL in 1 TUBE (51350-010-01) |
NDC Information of curacaine
| NDC Code | 51350-010-01 |
| Proprietary Name | curacaine |
| Package Description | 30 mL in 1 TUBE (51350-010-01) |
| Product NDC | 51350-010 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Lidocaine |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120912 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Transdermal Corp |
| Substance Name | LIDOCAINE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
