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Sodium Phenylbutyrate

NDC 49884-170, Sodium Phenylbutyrate Tablets, 500 mg, tablet, from Par Health USA, LLC.

Product NDC
49884-170
Status
Listed
Labeler
Par Health USA, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204395
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/49884-170 \
  -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
49884-170-04498840170041 BOTTLE in 1 CARTON (49884-170-04) / 250 TABLET in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4020b962-eaee-4184-b04b-14ca757c51a1

Use it

Look up 49884-170 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/49884-170 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 49884-170. 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.