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ATORVASTATIN CALCIUM

NDC 77771-453, ATORVASTATIN CALCIUM, tablet, film coated, from Radha Pharmaceuticals, Inc..

Product NDC
77771-453
Status
Listed
Labeler
Radha Pharmaceuticals, 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/77771-453 \
  -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
77771-453-10777710453101000 TABLET, FILM COATED in 1 BOTTLE (77771-453-10)
77771-453-907777104539090 TABLET, FILM COATED in 1 BOTTLE (77771-453-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/10e766cc-c3fd-4584-a0d7-652c516e828c

Use it

Look up 77771-453 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/77771-453 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 77771-453. 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.