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ATORVASTATIN CALCIUM

NDC 69097-898, ATORVASTATIN CALCIUM, tablet, film coated, from Cipla USA Inc.,.

Product NDC
69097-898
Status
Listed
Labeler
Cipla USA Inc.,
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205519
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69097-898 \
  -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
69097-898-056909708980590 TABLET, FILM COATED in 1 BOTTLE (69097-898-05)
69097-898-1269097089812500 TABLET, FILM COATED in 1 BOTTLE (69097-898-12)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/18fe5990-399d-416c-852f-e14974317b8b

Use it

Look up 69097-898 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69097-898 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69097-898. 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.