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NDC 58151-066, amlodipine and atorvastatin, tablet, film coated, from Viatris Specialty LLC.

Product NDC
58151-066
Status
Listed
Labeler
Viatris Specialty LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA021540
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/58151-066 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMLODIPINE BESYLATE5 mg/1
  • ATORVASTATIN CALCIUM TRIHYDRATE40 mg/1

Pharmacologic classes

Calcium Channel Antagonists [MoA]; Calcium Channel Blocker [EPC]; Cytochrome P450 3A Inhibitors [MoA]; Dihydropyridine Calcium Channel Blocker [EPC]; Dihydropyridines [CS]; HMG-CoA Reductase Inhibitor [EPC]; Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Package NDCNDC-11Package
58151-066-935815100669330 TABLET, FILM COATED in 1 BOTTLE (58151-066-93)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/164394b3-d7ba-4bbf-b64b-e2dd15735ea8

Use it

Look up 58151-066 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/58151-066 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 58151-066. 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.