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Deflazacort

NDC 70095-040, Deflazacort, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
70095-040
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217741
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70095-040 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DEFLAZACORT6 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70095-040-01700950040011 BOTTLE in 1 CARTON (70095-040-01) / 100 TABLET in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fb5350d5-ead1-41f4-8b25-0da0bd7fcffe

Use it

Look up 70095-040 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70095-040 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70095-040. 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.