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Simvastatin

NDC 70518-4102, Simvastatin, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-4102
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078034
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4102 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SIMVASTATIN5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70518-4102-07051841020030 TABLET, FILM COATED in 1 BLISTER PACK (70518-4102-0)
70518-4102-17051841020190 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4102-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/593f0007-9690-4de5-b1e9-59299e587643

Use it

Look up 70518-4102 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4102 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4102. 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.