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Deflazacort

NDC 70095-041, Deflazacort, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
70095-041
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/70095-041 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DEFLAZACORT18 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70095-041-30700950041301 BOTTLE in 1 CARTON (70095-041-30) / 30 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 70095-041 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70095-041 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70095-041. 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.