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SODIUM PHENYLACETATE AND SODIUM BENZOATE

NDC 70511-101, sodium phenylacetate and sodium benzoate, injection, solution, concentrate, from MAIA PHARMACEUTICALS, INC.

Product NDC
70511-101
Status
Listed
Labeler
MAIA PHARMACEUTICALS, INC
Dosage form
INJECTION, SOLUTION, CONCENTRATE
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208521
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70511-101 \
  -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
70511-101-50705110101501 VIAL, SINGLE-DOSE in 1 CARTON (70511-101-50) / 50 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3529be10-0004-4628-9ca1-67a8acd86b51

Use it

Look up 70511-101 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70511-101 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70511-101. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.