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SODIUM PHENYLACETATE and SODIUM BENZOATE

NDC 81665-203, sodium phenylacetate and sodium benzoate, injection, solution, concentrate, from Omnivium Pharmaceuticals LLC.

Product NDC
81665-203
Status
Listed
Labeler
Omnivium Pharmaceuticals LLC
Dosage form
INJECTION, SOLUTION, CONCENTRATE
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207096
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/81665-203 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM PHENYLACETATE100 mg/mL
  • SODIUM BENZOATE100 mg/mL

Pharmacologic classes

Ammonium Ion Binding Activity [MoA]; Ammonium Ion Binding Activity [MoA]; Nitrogen Binding Agent [EPC]; Nitrogen Binding Agent [EPC]

Package NDCNDC-11Package
81665-203-01816650203011 VIAL, SINGLE-DOSE in 1 CARTON (81665-203-01) / 50 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9067c301-74f9-457a-9b0f-b7e9b06a3508

Use it

Look up 81665-203 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/81665-203 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 81665-203. 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.