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ATORVASTATIN CALCIUM

NDC 50090-7358, ATORVASTATIN CALCIUM, tablet, film coated, from A-S Medication Solutions.

Product NDC
50090-7358
Status
Listed
Labeler
A-S Medication Solutions
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214344
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7358 \
  -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
50090-7358-05009073580030 TABLET, FILM COATED in 1 BOTTLE (50090-7358-0)
50090-7358-15009073580190 TABLET, FILM COATED in 1 BOTTLE (50090-7358-1)
50090-7358-250090735802100 TABLET, FILM COATED in 1 BOTTLE (50090-7358-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a4185ea4-8fc1-4af5-99b1-6e49f0c46463

Use it

Look up 50090-7358 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7358 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50090-7358. 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.