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Sodium phenylbutyrate

NDC 70710-2180, Sodium phenylbutyrate, tablet, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-2180
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA220418
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-2180 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM PHENYLBUTYRATE500 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70710-2180-8707102180081 BOTTLE in 1 CARTON (70710-2180-8) / 250 TABLET in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d08fd548-7eb8-4f6f-b664-b0fff6f30065

Use it

Look up 70710-2180 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-2180 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-2180. 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.