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ATORVASTATIN CALCIUM

NDC 71205-731, ATORVASTATIN CALCIUM, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-731
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207687
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-731 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ATORVASTATIN CALCIUM TRIHYDRATE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71205-731-307120507313030 TABLET, FILM COATED in 1 BOTTLE (71205-731-30)
71205-731-607120507316060 TABLET, FILM COATED in 1 BOTTLE (71205-731-60)
71205-731-907120507319090 TABLET, FILM COATED in 1 BOTTLE (71205-731-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a1b22973-cb9a-473e-a240-112b3e84e97c

Use it

Look up 71205-731 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-731 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-731. 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.