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Lovastatin

NDC 70518-2009, lovastatin, tablet, from REMEDYREPACK INC..

Product NDC
70518-2009
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078296
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2009 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LOVASTATIN20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70518-2009-07051820090090 TABLET in 1 BOTTLE, PLASTIC (70518-2009-0)
70518-2009-17051820090130 TABLET in 1 BLISTER PACK (70518-2009-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ff040b3c-6790-40d7-bd64-a4073b4a2045

Use it

Look up 70518-2009 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2009 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-2009. 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.