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6% HETASTARCH IN 0.9% SODIUM CHLORIDE

NDC 51662-1317, 6% HETASTARCH IN 0.9% SODIUM CHLORIDE, injection, solution, from HF Acquisition Co LLC, DBA HealthFirst.

Product NDC
51662-1317
Status
Listed
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
BA740193
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1317 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HETASTARCH6 g/100mL

Pharmacologic classes

Increased Intravascular Volume [PE]; Osmotic Activity [MoA]; Plasma Volume Expander [EPC]; Starch [CS]

Package NDCNDC-11Package
51662-1317-151662131701500 mL in 1 CONTAINER (51662-1317-1)
51662-1317-35166213170312 CONTAINER in 1 CASE (51662-1317-3) / 500 mL in 1 CONTAINER (51662-1317-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7b97c681-4514-c544-e053-2991aa0a3d78

Use it

Look up 51662-1317 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1317 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51662-1317. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.