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Clopidogrel

NDC 69367-200, Clopidogrel Bisulfate, tablet, film coated, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-200
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204165
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69367-200 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CLOPIDOGREL BISULFATE75 mg/1

Pharmacologic classes

Cytochrome P450 2C8 Inhibitors [MoA]; Decreased Platelet Aggregation [PE]; P2Y12 Platelet Inhibitor [EPC]; P2Y12 Receptor Antagonists [MoA]

Package NDCNDC-11Package
69367-200-0569367020005500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-200-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bb3b5e96-e629-4db5-8ad5-40c17c6dae18

  • NADAC price for package 69367020005

    GET /v1/drugs/nadac/69367020005

Use it

Look up 69367-200 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-200 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-200. 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.