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Sodium Acetate

NDC 0641-6262, Sodium Acetate, injection, from Hikma Pharmaceuticals USA Inc..

Product NDC
0641-6262
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216920
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0641-6262 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM ACETATE ANHYDROUS164 mg/mL

Pharmacologic classes

Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]

Package NDCNDC-11Package
0641-6262-01006416262011 VIAL in 1 CARTON (0641-6262-01) / 50 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7ee23a1c-bc99-4ff6-b2e7-d2aa42744553

Use it

Look up 0641-6262 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0641-6262 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0641-6262. 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.