NOREPINEPHRINE BITARTRATE injection, solution

Država: Združene države Amerike

Jezik: angleščina

Source: NLM (National Library of Medicine)

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Prenos Lastnosti izdelka (SPC)
06-03-2015

Aktivna sestavina:

Norepinephrine Bitartrate (UNII: IFY5PE3ZRW) (Norepinephrine - UNII:X4W3ENH1CV)

Dostopno od:

Cantrell Drug Company

INN (mednarodno ime):

Norepinephrine Bitartrate

Sestava:

Norepinephrine 16 ug in 1 mL

Pot uporabe:

INTRAVENOUS

Tip zastaranja:

PRESCRIPTION DRUG

Povzetek izdelek:

Norepinephrine bitartrate injection solution is supplied as a sterile, nonpyrogenic solution that is clear, colorless at 250 mL in a Single-Dose Injection Solution Bag. This product is Preservative-Free and Latex-Free.

Status dovoljenje:

unapproved drug other

Lastnosti izdelka

                                NOREPINEPHRINE BITARTRATE - NOREPINEPHRINE BITARTRATE INJECTION,
SOLUTION
CANTRELL DRUG COMPANY
_Disclaimer: This drug has not been found by FDA to be safe and
effective, and this labeling has not been_
_approved by FDA. For further information about unapproved drugs,
click here._
----------
NOREPINEPHRINE BITARTRATE 4 MG ADDED TO 5% DEXTROSE 250 ML BAG
• WARNINGS AND PRECAUTIONS
Outsourced Compounded Drug. Not for Resale. Hospital/Office Use Only.
• ADVERSE EVENTS
To facilitate Adverse Event Reporting: www.fda.gov/medwatch or
1-800-FDA-1088.
• HOW SUPPLIED
Norepinephrine bitartrate injection solution is supplied as a sterile,
nonpyrogenic solution that is clear,
colorless at 250 mL in a Single-Dose Injection Solution Bag.
This product is Preservative-Free and Latex-Free.
• INGREDIENTS
Each 1 mL contains the equivalent of 16 mcg norepinephrine base, 50 mg
dextrose, 118.4 mcg sodium
chloride, 32 mcg sodium metabisulfite, and pH adjusters include
hydrochloric acid and/or sodium
hydroxide, if necessary.
• STORAGE AND HANDLING
Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room
Temperature]. Protect from light.
Parenteral drug products should be inspected visually for particulate
matter and discoloration prior to
use, whenever solution and container permit.
Do not use the solution if its color is pinkish or darker than
slightly yellow or if it contains a
precipitate.
• DOSAGE AND ADMINISTRATION.
FOR INTRAVENOUS USE ONLY. PRESERVATIVE-FREE INJECTION SOLUTION.
RX ONLY
Rev. 03/15
CANTRELL DRUG COMPANY
LITTLE ROCK, AR 72207
NOREPINEPHRINE BITARTRATE
norepinephrine bitartrate injection, solution
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN PRESCRIPTION DRUG
ITE M CODE (SOURCE )
NDC:52533-16 5
ROUTE OF ADMINISTRATION
INTRAVENOUS
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
NO REPINEPHRINE BITA RTRA TE (UNII: IFY5PE3ZRW) (No repinephrine -
UNII:X4W3ENH1CV)
No re pine phrine
16 ug in 1 mL
Cantrell Drug Company
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
ANHYDRO US DEXTR
                                
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