HEPARIN SODIUM injection, solution

Land: Bandaríkin

Tungumál: enska

Heimild: NLM (National Library of Medicine)

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Download Vara einkenni (SPC)
15-05-2015

Virkt innihaldsefni:

Heparin Sodium (UNII: ZZ45AB24CA) (Heparin - UNII:T2410KM04A)

Fáanlegur frá:

Cantrell Drug Company

INN (Alþjóðlegt nafn):

Heparin Sodium

Samsetning:

Heparin 100 [USP'U] in 1 mL

Stjórnsýsluleið:

INTRAVENOUS

Gerð lyfseðils:

PRESCRIPTION DRUG

Vörulýsing:

Contains 25,000 USP Units of Heparin Sodium in 0.45% Sodium Chloride in a 250 mL Single-Dose Bag.  Volume & Concentration exlude additive & manufacturer overfill. This product is Sterile, Nonpyrogenic, and Latex Free.

Leyfisstaða:

unapproved drug other

Vara einkenni

                                HEPARIN SODIUM - HEPARIN SODIUM 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._
----------
HEPARIN SODIUM 25,000 USP UNITS ADDED TO 0.45% SODIUM CHLORIDE 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
Contains 25,000 USP Units of Heparin Sodium in 0.45% Sodium Chloride
in a 250 mL Single-Dose
Bag. Volume & Concentration exlude additive & manufacturer overfill.
This product is Sterile, Nonpyrogenic, and Latex Free.
• INGREDIENTS
Each 1 mL contains contains Heparin Sodium 100 USP Units, Sodium
Chloride 4.5 mg, Benzyl Alcohol
0.0002 mL. May contain Hydrochloric Acid and/or Sodium Hydroxide for
pH adjustment.
• STORAGE AND HANDLING
Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room
Temperature].
• DOSAGE AND ADMINISTRATION.
FOR INTRAVENOUS USE.
RX ONLY
Rev. 05/15
CANTRELL DRUG COMPANY
LITTLE ROCK, AR 72207
HEPARIN SODIUM
heparin sodium injection, solution
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN PRESCRIPTION DRUG
ITE M CODE (SOURCE )
NDC:52533-179
ROUTE OF ADMINISTRATION
INTRAVENOUS
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
HEPA RIN SO DIUM (UNII: ZZ45AB24CA) (Heparin - UNII:T2410 KM0 4A)
He pa rin
10 0 [USP'U] in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
SO DIUM CHLO RIDE (UNII: 451W47IQ8 X)
4.5 mg in 1 mL
BENZYL ALCO HO L (UNII: LKG8 49 4WBH)
0 .0 0 0 2 mL in 1 mL
WA TER (UNII: 0 59 QF0 KO0 R)
Cantrell Drug Company
OTHER INGREDIENTS
INGREDIENT KIND
INGREDIENT NAME
QUANTITY
May co ntain
HYDRO CHLO RIC ACID (UNII: QTT1758 2CB)
May co ntain
SO DIUM HYDRO XIDE (UNII: 55X0 4QC32I)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:52533-179 -18
250 mL in 1 BAG; Type 0
                                
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