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Lovastatin

NDC 71205-199, lovastatin, tablet, from Proficient Rx LP.

Product NDC
71205-199
Status
Listed
Labeler
Proficient Rx LP
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/71205-199 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LOVASTATIN40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71205-199-307120501993030 TABLET in 1 BOTTLE (71205-199-30)
71205-199-607120501996060 TABLET in 1 BOTTLE (71205-199-60)
71205-199-907120501999090 TABLET in 1 BOTTLE (71205-199-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/eb3b4051-3901-461d-a982-7ecd115ba669

Use it

Look up 71205-199 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-199 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-199. 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.