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Pirfenidone

NDC 70954-869, Pirfenidone, tablet, film coated, from ANI Pharmaceuticals, Inc..

Product NDC
70954-869
Status
Listed
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212722
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70954-869 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PIRFENIDONE267 mg/1

Pharmacologic classes

Pyridone [EPC]; Pyridones [CS]

Package NDCNDC-11Package
70954-869-10709540869103 BOTTLE in 1 CARTON (70954-869-10) / 90 TABLET, FILM COATED in 1 BOTTLE
70954-869-3070954086930270 TABLET, FILM COATED in 1 BOTTLE (70954-869-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/976620bb-c10e-4b13-8a97-7025fda6b7d5

  • NADAC price for package 70954086930

    GET /v1/drugs/nadac/70954086930

Use it

Look up 70954-869 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70954-869 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70954-869. 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.