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Sodium phenylacetate and Sodium benzoate

NDC 70710-1926, Sodium phenylacetate and Sodium benzoate, injection, solution, concentrate, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-1926
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
INJECTION, SOLUTION, CONCENTRATE
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217526
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1926 \
  -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
70710-1926-1707101926011 VIAL in 1 CARTON (70710-1926-1) / 20 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0f17c50f-3761-4470-bf3b-63837a287b8a

Use it

Look up 70710-1926 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1926 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1926. 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.