LidoPatch - 50682-527-03 - (lidocaine and menthol)

Alphabetical Index


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

Complete Information of LidoPatch


General Information