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LenzaPatch
LenzaPatch - 45861-017-05 - (LIDOCAINE HYDROCHLORIDE, MENTHOL)
Drug Information of LenzaPatch
| Product NDC: | 45861-017 |
| Proprietary Name: | LenzaPatch |
| Non Proprietary Name: | LIDOCAINE HYDROCHLORIDE, MENTHOL |
| Active Ingredient(s): | 4; 1 g/100g; g/100g & nbsp; LIDOCAINE HYDROCHLORIDE, MENTHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LenzaPatch
| Product NDC: | 45861-017 |
| Labeler Name: | Pharmaceutica North America, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130301 |
Package Information of LenzaPatch
| Package NDC: | 45861-017-05 |
| Package Description: | 5 PACKET in 1 BOX (45861-017-05) > 17 g in 1 PACKET |
NDC Information of LenzaPatch
| NDC Code | 45861-017-05 |
| Proprietary Name | LenzaPatch |
| Package Description | 5 PACKET in 1 BOX (45861-017-05) > 17 g in 1 PACKET |
| Product NDC | 45861-017 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | LIDOCAINE HYDROCHLORIDE, MENTHOL |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pharmaceutica North America, Inc. |
| Substance Name | LIDOCAINE HYDROCHLORIDE; MENTHOL |
| Strength Number | 4; 1 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |
