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FLUVASTATIN SODIUM ER

NDC 0781-8017, fluvastatin sodium, tablet, extended release, from Sandoz Inc.

Product NDC
0781-8017
Status
Listed
Labeler
Sandoz Inc
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA021192
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0781-8017 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUVASTATIN SODIUM80 mg/1

Pharmacologic classes

HMG-CoA Reductase Inhibitor [EPC]; Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Package NDCNDC-11Package
0781-8017-0100781801701100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-8017-01)
0781-8017-310078180173130 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-8017-31)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5ab4296c-87c2-4c64-b218-d620eef51310

  • NADAC price for package 00781801701

    GET /v1/drugs/nadac/00781801701

  • NADAC price for package 00781801731

    GET /v1/drugs/nadac/00781801731

Use it

Look up 0781-8017 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0781-8017 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0781-8017. 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.