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Pentoxifylline

NDC 70954-668, Pentoxifylline, tablet, extended release, from ANI Pharmaceuticals, Inc..

Product NDC
70954-668
Status
Listed
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074878
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70954-668 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PENTOXIFYLLINE400 mg/1

Pharmacologic classes

Blood Viscosity Reducer [EPC]; Hematologic Activity Alteration [PE]

Package NDCNDC-11Package
70954-668-1070954066810100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70954-668-10)
70954-668-2070954066820500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70954-668-20)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9ca79c97-e4e5-4297-85eb-7a9b3d8083b5

  • NADAC price for package 70954066810

    GET /v1/drugs/nadac/70954066810

  • NADAC price for package 70954066820

    GET /v1/drugs/nadac/70954066820

Use it

Look up 70954-668 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70954-668 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70954-668. 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.