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PRAVASTATIN SODIUM

NDC 67046-1519, PRAVASTATIN SODIUM, tablet, from Coupler LLC.

Product NDC
67046-1519
Status
Listed
Labeler
Coupler LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077987
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1519 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAVASTATIN SODIUM20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
67046-1519-36704615190330 TABLET in 1 BLISTER PACK (67046-1519-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2e07ad78-1059-e0ec-e063-6394a90a9bff

Use it

Look up 67046-1519 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1519 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67046-1519. 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.