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Chloroprocaine Hydrochloride - 55390-404-20 - (Chloroprocaine Hydrochloride)

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Drug Information of Chloroprocaine Hydrochloride

Product NDC: 55390-404
Proprietary Name: Chloroprocaine Hydrochloride
Non Proprietary Name: Chloroprocaine Hydrochloride
Active Ingredient(s): 30    mg/mL & nbsp;   Chloroprocaine Hydrochloride
Administration Route(s): EPIDURAL; INFILTRATION
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Chloroprocaine Hydrochloride

Product NDC: 55390-404
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040273
Marketing Category: ANDA
Start Marketing Date: 19981101

Package Information of Chloroprocaine Hydrochloride

Package NDC: 55390-404-20
Package Description: 1 VIAL in 1 BOX (55390-404-20) > 20 mL in 1 VIAL

NDC Information of Chloroprocaine Hydrochloride

NDC Code 55390-404-20
Proprietary Name Chloroprocaine Hydrochloride
Package Description 1 VIAL in 1 BOX (55390-404-20) > 20 mL in 1 VIAL
Product NDC 55390-404
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chloroprocaine Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name EPIDURAL; INFILTRATION
Start Marketing Date 19981101
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name CHLOROPROCAINE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/mL
Pharmaceutical Classes Ester Local Anesthetic [EPC],Esters [Chemical/Ingredient],Local Anesthesia [PE]

Complete Information of Chloroprocaine Hydrochloride


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