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Atorvastatin calcium

NDC 70518-3304, Atorvastatin calcium, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-3304
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211933
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3304 \
  -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
70518-3304-17051833040130 TABLET, FILM COATED in 1 BLISTER PACK (70518-3304-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/51e24220-3374-4e5e-9a8d-4113002c5bed

Use it

Look up 70518-3304 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3304 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3304. 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.