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Bupivacaine Hydrochloride - 0409-1161-01 - (BUPIVACAINE HYDROCHLORIDE)

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Drug Information of Bupivacaine Hydrochloride

Product NDC: 0409-1161
Proprietary Name: Bupivacaine Hydrochloride
Non Proprietary Name: BUPIVACAINE HYDROCHLORIDE
Active Ingredient(s): 5    mg/mL & nbsp;   BUPIVACAINE HYDROCHLORIDE
Administration Route(s): EPIDURAL; INTRACAUDAL
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Bupivacaine Hydrochloride

Product NDC: 0409-1161
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070609
Marketing Category: ANDA
Start Marketing Date: 20100107

Package Information of Bupivacaine Hydrochloride

Package NDC: 0409-1161-01
Package Description: 5 AMPULE in 1 CARTON (0409-1161-01) > 30 mL in 1 AMPULE

NDC Information of Bupivacaine Hydrochloride

NDC Code 0409-1161-01
Proprietary Name Bupivacaine Hydrochloride
Package Description 5 AMPULE in 1 CARTON (0409-1161-01) > 30 mL in 1 AMPULE
Product NDC 0409-1161
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BUPIVACAINE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name EPIDURAL; INTRACAUDAL
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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