Hetastarch in Sodium Chloride

Product NDC: 0409-7248
11-digit product format: 004097248
Labeler code: 0409
Product ID: 0409-7248_0a543f3b-31af-41aa-8c50-a30297aaae78
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: HETASTARCH
Dosage form: INJECTION, SOLUTION
Route: INTRAVENOUS
Labeler: Hospira, Inc.
Application: BA740193
Marketing category: ANDA
Marketing start: 2005-02-28
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: Hetastarch in Sodium Chloride
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 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
310757	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
d64f961a-3e1f-4b04-cf83-604474af2775	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0409-7248-03	Hetastarch in Sodium Chloride	12 in 1 CASE	INJECTION, SOLUTION	12		26
0409-7248-13	Hetastarch in Sodium Chloride	500 mL in 1 CONTAINER	INJECTION, SOLUTION	500		26

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0409-7248-03	ML - Milliliter	0409-7248	f4a893e5-da33-4f82-ba55-d29d608c39dd	1	2013-02-13
0409-7248-13	ML - Milliliter	0409-7248	9f143ead-9ea5-4918-b2ae-918d2b3de8f0	1	2016-07-19
0409-7248-49	ML - Milliliter	0409-7248	2819989f-8089-4315-bb13-bbf6dbaa4507	1	2013-02-13
0409-7248-59	ML - Milliliter	0409-7248	6b1435ff-001d-49a7-bab5-c5ebaf805af2	1	2018-03-08

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
HETASTARCH	ACTIVE INGREDIENT	875Y4127EA	HETASTARCH IN SODIUM CHLORIDE (HETASTARCH) INJECTION, SOLUTION [HOSPIRA, INC.]	12
HETASTARCH	ACTIVE MOIETY	875Y4127EA	HETASTARCH IN SODIUM CHLORIDE (HETASTARCH) INJECTION, SOLUTION [HOSPIRA, INC.]	12
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	HETASTARCH IN SODIUM CHLORIDE (HETASTARCH) INJECTION, SOLUTION [HOSPIRA, INC.]	12
SODIUM HYDROXIDE	INACTIVE INGREDIENT	55X04QC32I	HETASTARCH IN SODIUM CHLORIDE (HETASTARCH) INJECTION, SOLUTION [HOSPIRA, INC.]	12
WATER	INACTIVE INGREDIENT	059QF0KO0R	HETASTARCH IN SODIUM CHLORIDE (HETASTARCH) INJECTION, SOLUTION [HOSPIRA, INC.]	12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0409-7248	HETASTARCH IN SODIUM CHLORIDE (HETASTARCH) INJECTION, SOLUTION [HOSPIRA, INC.]	22	Current NDC, Legacy NDC, 2 package rows	20250221_d64f961a-3e1f-4b04-cf83-604474af2775.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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hetastarch in Sodium Chloride	HETASTARCH	Hospira, Inc.	d64f961a-3e1f-4b04-cf83-604474af2775	2026-04-30	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: BA740193 ndc (product): 0409-7248
6% HETASTARCH IN 0.9% SODIUM CHLORIDE	6% HETASTARCH IN 0.9% SODIUM CHLORIDE	HF Acquisition Co LLC, DBA HealthFirst	7b97c681-4514-c544-e053-2991aa0a3d78	2024-01-29	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: BA740193

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
875Y4127EA	HETASTARCH	9005-27-0	HETASTARCH

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
310757	hetastarch 6 % in 500 ML Injection	PSN	d64f961a-3e1f-4b04-cf83-604474af2775	26
310757	500 ML hetastarch 60 MG/ML Injection	SCD	d64f961a-3e1f-4b04-cf83-604474af2775	26
310757	hetastarch 6 % per 500 ML Injection	SY	d64f961a-3e1f-4b04-cf83-604474af2775	26
310757	hetastarch 6 % in 500 ML Injection	PSN	7b97c681-4514-c544-e053-2991aa0a3d78	6
310757	500 ML hetastarch 60 MG/ML Injection	SCD	7b97c681-4514-c544-e053-2991aa0a3d78	6
310757	hetastarch 6 % per 500 ML Injection	SY	7b97c681-4514-c544-e053-2991aa0a3d78	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0409-7248-03	00409724803	12 CONTAINER in 1 CASE (0409-7248-03) / 500 mL in 1 CONTAINER (0409-7248-13)	12 container	2005-02-28	0000-00-00	No	No	Current
0409-7248-13	00409724813	500 mL in 1 CONTAINER	500 ml					Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Hetastarch in Sodium Chloride	Hospira, Inc.	2026-04-30	HUMAN PRESCRIPTION DRUG LABEL	26
6% HETASTARCH IN 0.9% SODIUM CHLORIDE INJECTION 500mL BAG	HF Acquisition Co LLC, DBA HealthFirst	2024-01-29	HUMAN PRESCRIPTION DRUG LABEL	6