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SENSORCAINE - 63323-472-37 - (BUPIVACAINE HYDROCHLORIDE)

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Drug Information of SENSORCAINE

Product NDC: 63323-472
Proprietary Name: SENSORCAINE
Non Proprietary Name: BUPIVACAINE HYDROCHLORIDE
Active Ingredient(s): 7.5    mg/mL & nbsp;   BUPIVACAINE HYDROCHLORIDE
Administration Route(s): EPIDURAL; RETROBULBAR
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of SENSORCAINE

Product NDC: 63323-472
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070554
Marketing Category: ANDA
Start Marketing Date: 20101119

Package Information of SENSORCAINE

Package NDC: 63323-472-37
Package Description: 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-472-37) > 30 mL in 1 VIAL, SINGLE-DOSE

NDC Information of SENSORCAINE

NDC Code 63323-472-37
Proprietary Name SENSORCAINE
Package Description 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-472-37) > 30 mL in 1 VIAL, SINGLE-DOSE
Product NDC 63323-472
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BUPIVACAINE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name EPIDURAL; RETROBULBAR
Start Marketing Date 20101119
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name BUPIVACAINE HYDROCHLORIDE
Strength Number 7.5
Strength Unit mg/mL
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE]

Complete Information of SENSORCAINE


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