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
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 NDC | NDC-11 | Package |
|---|---|---|
| 70511-101-50 | 70511010150 | 1 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 https://api.healthcare.dev/v1/drugs/ndc/70511-101 \ -H "Authorization: Bearer $HDEV_API_KEY"
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.