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SIMVASTATIN

NDC 71205-192, SIMVASTATIN, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-192
Status
Listed
Labeler
Proficient Rx LP
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/71205-192 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SIMVASTATIN40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71205-192-307120501923030 TABLET, FILM COATED in 1 BOTTLE (71205-192-30)
71205-192-607120501926060 TABLET, FILM COATED in 1 BOTTLE (71205-192-60)
71205-192-907120501929090 TABLET, FILM COATED in 1 BOTTLE (71205-192-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7649bec7-04c6-47b5-a050-15923006dac0

Use it

Look up 71205-192 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-192 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-192. 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.