Home NDC 0409-1555 Hextend
Product NDC 0409-1555
11-digit product format 004091555
Labeler code 0409
Product ID 0409-1555_9829894c-8ff3-4355-94d1-1cd61363db2c
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name HETASTARCH
Dosage form INJECTION, SOLUTION
Route INTRAVENOUS
Labeler Hospira, Inc.
Application BN200952
Marketing category NDA
Marketing start 2005-02-02
Substance HETASTARCH
Active strength 6 g/100mL
Pharmacologic classes Increased Intravascular Volume [PE], Osmotic Activity [MoA], Plasma Volume Expander [EPC], Starch [CS]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Hextend
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HETASTARCH 6 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 875Y4127EA Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 310757 Internal RxNorm lookup 404665 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0409-1555-54 Hextend 12 in 1 CASE INJECTION, SOLUTION 12 25 0409-1555-64 Hextend 500 mL in 1 BAG INJECTION, SOLUTION 500 25
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded HETASTARCH ACTIVE INGREDIENT 875Y4127EA HEXTEND (HETASTARCH) INJECTION, SOLUTION [HOSPIRA, INC.] 13 HETASTARCH ACTIVE MOIETY 875Y4127EA HEXTEND (HETASTARCH) INJECTION, SOLUTION [HOSPIRA, INC.] 13 CALCIUM CHLORIDE INACTIVE INGREDIENT M4I0D6VV5M HEXTEND (HETASTARCH) INJECTION, SOLUTION [HOSPIRA, INC.] 13 DEXTROSE MONOHYDRATE INACTIVE INGREDIENT LX22YL083G HEXTEND (HETASTARCH) INJECTION, SOLUTION [HOSPIRA, INC.] 13 MAGNESIUM CHLORIDE INACTIVE INGREDIENT 02F3473H9O HEXTEND (HETASTARCH) INJECTION, SOLUTION [HOSPIRA, INC.] 13 POTASSIUM CHLORIDE INACTIVE INGREDIENT 660YQ98I10 HEXTEND (HETASTARCH) INJECTION, SOLUTION [HOSPIRA, INC.] 13 SODIUM CHLORIDE INACTIVE INGREDIENT 451W47IQ8X HEXTEND (HETASTARCH) INJECTION, SOLUTION [HOSPIRA, INC.] 13 SODIUM LACTATE INACTIVE INGREDIENT TU7HW0W0QT HEXTEND (HETASTARCH) INJECTION, SOLUTION [HOSPIRA, INC.] 13 WATER INACTIVE INGREDIENT 059QF0KO0R HEXTEND (HETASTARCH) INJECTION, SOLUTION [HOSPIRA, INC.] 13
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0409-1555 HEXTEND (HETASTARCH) INJECTION, SOLUTION [HOSPIRA, INC.] 22 Current NDC, Legacy NDC, 2 package rows 20250110_fc79700c-6c3b-4998-8307-4dc8c81c5041.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 0409-1555-54 00409155554 12 BAG in 1 CASE (0409-1555-54) / 500 mL in 1 BAG (0409-1555-64) 12 bag 2005-02-02 0000-00-00 No No Current 0409-1555-64 00409155564 500 mL in 1 BAG 500 ml Historical