NDC 55150-233 – Fondaparinux Sodium

Fondaparinux Sodium 10 mg/.8mL · Injection, Solution · Subcutaneous

Human Prescription Drug 1 recall

Product NDC55150-233

Product details

Brand name
Fondaparinux Sodium
Generic name
Fondaparinux Sodium
Labeler
Eugia US LLC
Dosage form
Injection, Solution
Route
Subcutaneous
Marketing category
ANDA · ANDA206918
Marketed since
December 26, 2017
Listing expires
December 31, 2026
Pharmacologic class
Factor Xa Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fondaparinux Sodium →

Package NDC codes (2)

Package NDCDescriptionSince
55150-233-022 SYRINGE, GLASS in 1 CARTON (55150-233-02) / .8 mL in 1 SYRINGE, GLASS (55150-233-00)Dec 26, 2017
55150-233-1010 SYRINGE, GLASS in 1 CARTON (55150-233-10) / .8 mL in 1 SYRINGE, GLASS (55150-233-00)Dec 26, 2017

Recalls mentioning this NDC

Other Fondaparinux Sodium products