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SIMVASTATIN

NDC 42708-169, SIMVASTATIN, tablet, film coated, from QPharma, Inc.

Product NDC
42708-169
Status
Listed
Labeler
QPharma, Inc
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078103
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42708-169 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SIMVASTATIN20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
42708-169-304270801693030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-169-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f71fc0ac-223e-18c1-e053-6394a90a45ca

Use it

Look up 42708-169 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42708-169 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42708-169. 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.