PLIAGLIS - 0299-6100-35 - (lidocaine and tetracaine)

Alphabetical Index


Drug Information of PLIAGLIS

Product NDC: 0299-6100
Proprietary Name: PLIAGLIS
Non Proprietary Name: lidocaine and tetracaine
Active Ingredient(s): 70; 70    mg/g; mg/g & nbsp;   lidocaine and tetracaine
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of PLIAGLIS

Product NDC: 0299-6100
Labeler Name: Galderma Laboratories, L.P.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021717
Marketing Category: NDA
Start Marketing Date: 20060629

Package Information of PLIAGLIS

Package NDC: 0299-6100-35
Package Description: 30 g in 1 TUBE (0299-6100-35)

NDC Information of PLIAGLIS

NDC Code 0299-6100-35
Proprietary Name PLIAGLIS
Package Description 30 g in 1 TUBE (0299-6100-35)
Product NDC 0299-6100
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lidocaine and tetracaine
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20060629
Marketing Category Name NDA
Labeler Name Galderma Laboratories, L.P.
Substance Name LIDOCAINE; TETRACAINE
Strength Number 70; 70
Strength Unit mg/g; mg/g
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE],Ester Local Anesthetic [EPC],Esters [Chemical/Ingredient],Local Anesthesia [PE]

Complete Information of PLIAGLIS


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