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LidoPatch
LidoPatch - 50682-527-03 - (lidocaine and menthol)
Drug Information of LidoPatch
| Product NDC: | 50682-527 |
| Proprietary Name: | LidoPatch |
| Non Proprietary Name: | lidocaine and menthol |
| Active Ingredient(s): | 40; 50 mg/1; mg/1 & nbsp; lidocaine and menthol |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | PATCH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LidoPatch
| Product NDC: | 50682-527 |
| Labeler Name: | 3T Federal Solutions LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120201 |
Package Information of LidoPatch
| Package NDC: | 50682-527-03 |
| Package Description: | 3 POUCH in 1 CARTON (50682-527-03) > 1 PATCH in 1 POUCH |
NDC Information of LidoPatch
| NDC Code | 50682-527-03 |
| Proprietary Name | LidoPatch |
| Package Description | 3 POUCH in 1 CARTON (50682-527-03) > 1 PATCH in 1 POUCH |
| Product NDC | 50682-527 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | lidocaine and menthol |
| Dosage Form Name | PATCH |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 20120201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | 3T Federal Solutions LLC |
| Substance Name | LIDOCAINE; MENTHOL |
| Strength Number | 40; 50 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
