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Sodium acetate anhydrous

NDC 70069-048, Sodium acetate anhydrous, solution, concentrate, from Somerset Therapeutics, LLC.

Product NDC
70069-048
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
SOLUTION, CONCENTRATE
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219826
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-048 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM ACETATE ANHYDROUS164 mg/mL
Package NDCNDC-11Package
70069-048-207006900482020 VIAL, GLASS in 1 CARTON (70069-048-20) / 100 mL in 1 VIAL, GLASS

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/93edebd6-ef7f-483a-80b6-bfaf34ea5ded

Use it

Look up 70069-048 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-048 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-048. 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.