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Sodium Phenylbutyrate

NDC 49884-006, Sodium Phenylbutyrate, powder, from Par Health USA, LLC.

Product NDC
49884-006
Status
Listed
Labeler
Par Health USA, LLC
Dosage form
POWDER
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203918
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/49884-006 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM PHENYLBUTYRATE.94 g/g

Pharmacologic classes

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

Package NDCNDC-11Package
49884-006-04498840006041 BOTTLE in 1 CARTON (49884-006-04) / 250 g in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/639f5c7e-9f6d-47fb-a417-2be076176a78

Use it

Look up 49884-006 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/49884-006 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 49884-006. 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.