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SENSORCAINE - 63323-468-37 - (BUPIVACAINE HYDROCHLORIDE,EPINEPHRINE BITARTRATE)

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Drug Information of SENSORCAINE

Product NDC: 63323-468
Proprietary Name: SENSORCAINE
Non Proprietary Name: BUPIVACAINE HYDROCHLORIDE,EPINEPHRINE BITARTRATE
Active Ingredient(s): 2.5; .0091    mg/mL; mg/mL & nbsp;   BUPIVACAINE HYDROCHLORIDE,EPINEPHRINE BITARTRATE
Administration Route(s): EPIDURAL; INFILTRATION; INTRACAUDAL; PERINEURAL
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of SENSORCAINE

Product NDC: 63323-468
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070966
Marketing Category: ANDA
Start Marketing Date: 20101119

Package Information of SENSORCAINE

Package NDC: 63323-468-37
Package Description: 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-468-37) > 30 mL in 1 VIAL, SINGLE-DOSE

NDC Information of SENSORCAINE

NDC Code 63323-468-37
Proprietary Name SENSORCAINE
Package Description 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-468-37) > 30 mL in 1 VIAL, SINGLE-DOSE
Product NDC 63323-468
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BUPIVACAINE HYDROCHLORIDE,EPINEPHRINE BITARTRATE
Dosage Form Name INJECTION, SOLUTION
Route Name EPIDURAL; INFILTRATION; INTRACAUDAL; PERINEURAL
Start Marketing Date 20101119
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name BUPIVACAINE HYDROCHLORIDE; EPINEPHRINE BITARTRATE
Strength Number 2.5; .0091
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE],Adrenergic alpha-Agonists [MoA],Adrenergic beta-Agonists [MoA],alpha-Adrenergic Agonist [EPC],beta-Adrenergic Agonist [EPC],Catecholamine [EPC],Catecholamines [Chemical/Ingredient]

Complete Information of SENSORCAINE


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