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Fluvastatin Sodium

NDC 0093-7446, Fluvastatin Sodium, tablet, film coated, extended release, from Teva Pharmaceuticals USA, Inc..

Product NDC
0093-7446
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA079011
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0093-7446 \
  -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
0093-7446-0100093744601100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7446-01)
0093-7446-560009374465630 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7446-56)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cc55110f-1ad6-4f97-840d-62b3a5ac415a

  • NADAC price for package 00093744601

    GET /v1/drugs/nadac/00093744601

  • NADAC price for package 00093744656

    GET /v1/drugs/nadac/00093744656

Use it

Look up 0093-7446 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0093-7446 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0093-7446. 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.