NDC Product
Human Prescription Drug6% Hetastarch In 0.9% Sodium Chloride NDC 51662-1317
- Generic Name
- 6% Hetastarch In 0.9% Sodium Chloride
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
HETASTARCH
UNII 875Y4127EA
Substance Identification & Data
This profile provides standardized clinical and technical data for Hetastarch, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 875Y4127EA.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9005-27-0 and the RxNorm Concept ID (RxCUI) 5531. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
HETASTARCH
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
875Y4127EA
The specific atomic composition represented as a molecular structure string.
Substance Type
polymer
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Hetastarch. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.
FDA Official Name
HETASTARCH
Common Names & Synonyms
HETASTARCH [II]
HETASTARCH [MI]
HETASTARCH [USAN]
HETASTARCH [VANDF]
HETASTARCH [WHO-DD]
HYDROXYETHYL STARCH
HYDROXYETHYL STARCH [VANDF]
STARCH 2-HYDROXYETHYL ETHER
STARCH, 2-HYDROXYETHYL ETHER
Brand / Trade Names
HESPAN
NDC Products Containing HETASTARCH
This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory:
