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Simvastatin

NDC 71205-780, Simvastatin, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-780
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077691
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-780 \
  -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
71205-780-307120507803030 TABLET, FILM COATED in 1 BOTTLE (71205-780-30)
71205-780-607120507806060 TABLET, FILM COATED in 1 BOTTLE (71205-780-60)
71205-780-907120507809090 TABLET, FILM COATED in 1 BOTTLE (71205-780-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b5b47d5b-f953-4e82-99ef-e4e10164095e

Use it

Look up 71205-780 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-780 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-780. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.