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Atorvastatin calcium

NDC 60290-041, Atorvastatin calcium, tablet, from Umedica Laboratories USA Inc..

Product NDC
60290-041
Status
Listed
Labeler
Umedica Laboratories USA Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213853
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60290-041 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ATORVASTATIN40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
60290-041-016029000410190 TABLET in 1 BOTTLE (60290-041-01)
60290-041-0260290004102500 TABLET in 1 BOTTLE (60290-041-02)
60290-041-03602900041032500 TABLET in 1 BOTTLE (60290-041-03)
60290-041-04602900041041000 TABLET in 1 BOTTLE (60290-041-04)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5a7594ca-30be-4350-827f-ef745a2a7e18

Use it

Look up 60290-041 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60290-041 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60290-041. 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.