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Budesonide

NDC 0591-2510, Budesonide, tablet, film coated, extended release, from Actavis Pharma, Inc..

Product NDC
0591-2510
Status
Listed
Labeler
Actavis Pharma, Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205457
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0591-2510 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUDESONIDE9 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
0591-2510-300059125103030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-2510-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/41d4fd39-81ee-41be-b34d-efb12b3a359d

  • NADAC price for package 00591251030

    GET /v1/drugs/nadac/00591251030

Use it

Look up 0591-2510 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0591-2510 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0591-2510. 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.