Land: Bandaríkin
Tungumál: enska
Heimild: NLM (National Library of Medicine)
Heparin Sodium (UNII: ZZ45AB24CA) (Heparin - UNII:T2410KM04A)
Cantrell Drug Company
Heparin Sodium
Heparin 100 [USP'U] in 1 mL
INTRAVENOUS
PRESCRIPTION DRUG
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.
unapproved drug other
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 Lestu allt skjalið