Xylocaine - 66312-181-16 - (Lidocaine Hydrochloride and Epinephrine Bitartrate)

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Drug Information of Xylocaine

Product NDC: 66312-181
Proprietary Name: Xylocaine
Non Proprietary Name: Lidocaine Hydrochloride and Epinephrine Bitartrate
Active Ingredient(s): 20; 20    ug/mL; mg/mL & nbsp;   Lidocaine Hydrochloride and Epinephrine Bitartrate
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Xylocaine

Product NDC: 66312-181
Labeler Name: Dentsply Pharmaceutical
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA088389
Marketing Category: NDA
Start Marketing Date: 19850122

Package Information of Xylocaine

Package NDC: 66312-181-16
Package Description: 50 CARTRIDGE in 1 CARTON (66312-181-16) > 1.7 mL in 1 CARTRIDGE

NDC Information of Xylocaine

NDC Code 66312-181-16
Proprietary Name Xylocaine
Package Description 50 CARTRIDGE in 1 CARTON (66312-181-16) > 1.7 mL in 1 CARTRIDGE
Product NDC 66312-181
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine Hydrochloride and Epinephrine Bitartrate
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19850122
Marketing Category Name NDA
Labeler Name Dentsply Pharmaceutical
Substance Name EPINEPHRINE BITARTRATE; LIDOCAINE HYDROCHLORIDE
Strength Number 20; 20
Strength Unit ug/mL; mg/mL
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE],Adrenergic alpha-Agonists [MoA],Adrenergic beta-Agonists [MoA],alpha-Adrenergic Agonist [EPC],beta-Adrenergic Agonist [EPC],Catecholamine [EPC],Catecholamines [Chemical/Ingredient]

Complete Information of Xylocaine


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