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Bupivacaine Hydrochloride - 0409-1163-01 - (BUPIVACAINE HYDROCHLORIDE)

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Drug Information of Bupivacaine Hydrochloride

Product NDC: 0409-1163
Proprietary Name: Bupivacaine Hydrochloride
Non Proprietary Name: BUPIVACAINE HYDROCHLORIDE
Active Ingredient(s): 5    mg/mL & nbsp;   BUPIVACAINE HYDROCHLORIDE
Administration Route(s): INFILTRATION
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Bupivacaine Hydrochloride

Product NDC: 0409-1163
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070597
Marketing Category: ANDA
Start Marketing Date: 20100107

Package Information of Bupivacaine Hydrochloride

Package NDC: 0409-1163-01
Package Description: 25 VIAL, MULTI-DOSE in 1 TRAY (0409-1163-01) > 50 mL in 1 VIAL, MULTI-DOSE

NDC Information of Bupivacaine Hydrochloride

NDC Code 0409-1163-01
Proprietary Name Bupivacaine Hydrochloride
Package Description 25 VIAL, MULTI-DOSE in 1 TRAY (0409-1163-01) > 50 mL in 1 VIAL, MULTI-DOSE
Product NDC 0409-1163
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BUPIVACAINE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INFILTRATION
Start Marketing Date 20100107
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name BUPIVACAINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE]

Complete Information of Bupivacaine Hydrochloride


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