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atorvastatin calcium

NDC 82137-017, atorvastatin calcium, tablet, film coated, from Lepu Pharmaceutical Technology Co., Ltd..

Product NDC
82137-017
Status
Listed
Labeler
Lepu Pharmaceutical Technology Co., Ltd.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216848
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82137-017 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ATORVASTATIN CALCIUM TRIHYDRATE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
82137-017-018213700170190 TABLET, FILM COATED in 1 BOTTLE (82137-017-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/173474b6-26b4-46f2-a12a-64753ae5e905

Use it

Look up 82137-017 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82137-017 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82137-017. 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.