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Atorvastatin Calcium

NDC 81033-514, Atorvastatin Calcium, tablet, film coated, from Kesin Pharma Corporation.

Product NDC
81033-514
Status
Listed
Labeler
Kesin Pharma Corporation
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209288
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/81033-514 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ATORVASTATIN CALCIUM TRIHYDRATE80 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
81033-514-018103305140110 BLISTER PACK in 1 CARTON (81033-514-01) / 100 TABLET, FILM COATED in 1 BLISTER PACK (81033-514-40)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/56826bb5-ae70-af65-e063-6294a90abf74

Use it

Look up 81033-514 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/81033-514 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 81033-514. 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.