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sodium phenylbutyrate

NDC 68462-853, sodium phenylbutyrate, tablet, from GLENMARK PHARMACEUTICALS INC., USA.

Product NDC
68462-853
Status
Listed
Labeler
GLENMARK PHARMACEUTICALS INC., USA
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216462
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68462-853 \
  -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
68462-853-2068462085320250 TABLET in 1 BOTTLE (68462-853-20)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0c76d25b-abac-41a3-a547-4fa4796bf7a4

Use it

Look up 68462-853 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68462-853 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68462-853. 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.