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LMX5
LMX5 - 0496-0883-30 - (lidocaine)
Drug Information of LMX5
| Product NDC: | 0496-0883 |
| Proprietary Name: | LMX5 |
| Non Proprietary Name: | lidocaine |
| Active Ingredient(s): | 50 mg/g & nbsp; lidocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LMX5
| Product NDC: | 0496-0883 |
| Labeler Name: | Ferndale Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20031001 |
Package Information of LMX5
| Package NDC: | 0496-0883-30 |
| Package Description: | 30 g in 1 TUBE (0496-0883-30) |
NDC Information of LMX5
| NDC Code | 0496-0883-30 |
| Proprietary Name | LMX5 |
| Package Description | 30 g in 1 TUBE (0496-0883-30) |
| Product NDC | 0496-0883 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | lidocaine |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20031001 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ferndale Laboratories, Inc. |
| Substance Name | LIDOCAINE |
| Strength Number | 50 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
