NDC 0409-1555 – Hextend

Hetastarch 6 g/100mL · Injection, Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC0409-1555

Product details

Brand name
Hextend
Generic name
Hetastarch
Labeler
Hospira, Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
NDA · BN200952
Marketed since
February 2, 2005
Listing expires
December 31, 2027
Pharmacologic class
Plasma Volume Expander

Active ingredients

Uses, dosage, side effects and warnings for Hextend →

Package NDC codes (1)

Package NDCDescriptionSince
0409-1555-5412 BAG in 1 CASE (0409-1555-54) / 500 mL in 1 BAG (0409-1555-64)Feb 2, 2005

Recalls mentioning this NDC