United States · FDA National Drug Code directory
Hetastarch in Sodium Chloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0409-7248_0a543f3b-31af-41aa-8c50-a30297aaae78
- Product NDC
- 0409-7248
- Form
- INJECTION, SOLUTION
- Composition / generic term
- HETASTARCH
- Labeler
- Hospira, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20050228
- Source listing expiry
- 20271231
Source-listed ingredients
- HETASTARCH — 6 g/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 12 CONTAINER in 1 CASE (0409-7248-03) / 500 mL in 1 CONTAINER (0409-7248-13) · 0409-7248-03
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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