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Simvastatin

NDC 70518-3630, Simvastatin, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-3630
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078034
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3630 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SIMVASTATIN20 mg/1

Pharmacologic classes

HMG-CoA Reductase Inhibitor [EPC]; Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Package NDCNDC-11Package
70518-3630-07051836300030 TABLET, FILM COATED in 1 BLISTER PACK (70518-3630-0)
70518-3630-17051836300190 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3630-1)
70518-3630-37051836300320 TABLET, FILM COATED in 1 BLISTER PACK (70518-3630-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d053fee4-b797-4a82-8865-0b4d08b14990

Use it

Look up 70518-3630 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3630 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3630. 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.