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Budesonide

NDC 60687-889, Budesonide, suspension, from American Health Packaging.

Product NDC
60687-889
Status
Listed
Labeler
American Health Packaging
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/60687-889 \
  -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
60687-889-836068708898330 POUCH in 1 CARTON (60687-889-83) / 1 AMPULE in 1 POUCH (60687-889-79) / 2 mL in 1 AMPULE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c7df2a10-4166-423e-bb60-5f3a8234f26c

  • NADAC price for package 60687088983

    GET /v1/drugs/nadac/60687088983

Use it

Look up 60687-889 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60687-889 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60687-889. 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.