EMLA - 76478-289-30 - (lidocaine and prilocaine)

Alphabetical Index


Drug Information of EMLA

Product NDC: 76478-289
Proprietary Name: EMLA
Non Proprietary Name: lidocaine and prilocaine
Active Ingredient(s): 25; 25    mg/g; mg/g & nbsp;   lidocaine and prilocaine
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of EMLA

Product NDC: 76478-289
Labeler Name: Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.)
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019941
Marketing Category: NDA
Start Marketing Date: 20121112

Package Information of EMLA

Package NDC: 76478-289-30
Package Description: 1 TUBE in 1 CARTON (76478-289-30) > 30 g in 1 TUBE

NDC Information of EMLA

NDC Code 76478-289-30
Proprietary Name EMLA
Package Description 1 TUBE in 1 CARTON (76478-289-30) > 30 g in 1 TUBE
Product NDC 76478-289
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lidocaine and prilocaine
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20121112
Marketing Category Name NDA
Labeler Name Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.)
Substance Name LIDOCAINE; PRILOCAINE
Strength Number 25; 25
Strength Unit mg/g; mg/g
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE],Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE]

Complete Information of EMLA


General Information