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Budesonide

NDC 47335-631, Budesonide, suspension, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-631
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
SUSPENSION
Route
RESPIRATORY (INHALATION)
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211922
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-631 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUDESONIDE.25 mg/2mL

Pharmacologic classes

Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]

Package NDCNDC-11Package
47335-631-49473350631496 POUCH in 1 CARTON (47335-631-49) / 5 AMPULE in 1 POUCH (47335-631-48) / 2 mL in 1 AMPULE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a39fbcfc-3ffd-44bd-b882-01f8e1844213

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=47335-631

  • NADAC price for package 47335063149

    GET /v1/drugs/nadac/47335063149

Use it

Look up 47335-631 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-631 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-631. 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.