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Sodium Acetate

NDC 71357-008, Sodium Acetate Injection, USP, 200 mEq/100 mL, injection, solution, concentrate, from MILLA PHARMACEUTICALS INC..

Product NDC
71357-008
Status
Listed
Labeler
MILLA PHARMACEUTICALS INC.
Dosage form
INJECTION, SOLUTION, CONCENTRATE
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214805
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71357-008 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM ACETATE200 meq/100mL
Package NDCNDC-11Package
71357-008-107135700081010 VIAL, PHARMACY BULK PACKAGE in 1 CASE (71357-008-10) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (71357-008-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1ea1466d-a492-4056-e063-6394a90a80bf

Use it

Look up 71357-008 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71357-008 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71357-008. 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.