Nesacaine - 63323-475-37 - (CHLOROPROCAINE HYDROCHLORIDE)

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Drug Information of Nesacaine

Product NDC: 63323-475
Proprietary Name: Nesacaine
Non Proprietary Name: CHLOROPROCAINE HYDROCHLORIDE
Active Ingredient(s): 10    mg/mL & nbsp;   CHLOROPROCAINE HYDROCHLORIDE
Administration Route(s): INFILTRATION; PERINEURAL
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nesacaine

Product NDC: 63323-475
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA009435
Marketing Category: NDA
Start Marketing Date: 20101014

Package Information of Nesacaine

Package NDC: 63323-475-37
Package Description: 25 VIAL, MULTI-DOSE in 1 CARTON (63323-475-37) > 30 mL in 1 VIAL, MULTI-DOSE

NDC Information of Nesacaine

NDC Code 63323-475-37
Proprietary Name Nesacaine
Package Description 25 VIAL, MULTI-DOSE in 1 CARTON (63323-475-37) > 30 mL in 1 VIAL, MULTI-DOSE
Product NDC 63323-475
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CHLOROPROCAINE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INFILTRATION; PERINEURAL
Start Marketing Date 20101014
Marketing Category Name NDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name CHLOROPROCAINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Ester Local Anesthetic [EPC],Esters [Chemical/Ingredient],Local Anesthesia [PE]

Complete Information of Nesacaine


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