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Norepinephrine Bitartrate - 52533-165-38 - (Norepinephrine Bitartrate)

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Drug Information of Norepinephrine Bitartrate

Product NDC: 52533-165
Proprietary Name: Norepinephrine Bitartrate
Non Proprietary Name: Norepinephrine Bitartrate
Active Ingredient(s): 16    ug/mL & nbsp;   Norepinephrine Bitartrate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Norepinephrine Bitartrate

Product NDC: 52533-165
Labeler Name: Cantrell Drug Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120412

Package Information of Norepinephrine Bitartrate

Package NDC: 52533-165-38
Package Description: 250 mL in 1 BAG (52533-165-38)

NDC Information of Norepinephrine Bitartrate

NDC Code 52533-165-38
Proprietary Name Norepinephrine Bitartrate
Package Description 250 mL in 1 BAG (52533-165-38)
Product NDC 52533-165
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Norepinephrine Bitartrate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120412
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Cantrell Drug Company
Substance Name NOREPINEPHRINE BITARTRATE
Strength Number 16
Strength Unit ug/mL
Pharmaceutical Classes Catecholamine [EPC],Catecholamines [Chemical/Ingredient]

Complete Information of Norepinephrine Bitartrate


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