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Prasugrel

NDC 65862-829, Prasugrel, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
65862-829
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205888
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-829 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRASUGREL HYDROCHLORIDE5 mg/1

Pharmacologic classes

Decreased Platelet Aggregation [PE]; P2Y12 Platelet Inhibitor [EPC]; P2Y12 Receptor Antagonists [MoA]

Package NDCNDC-11Package
65862-829-03658620829033 BLISTER PACK in 1 CARTON (65862-829-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-829-10)
65862-829-306586208293030 TABLET, FILM COATED in 1 BOTTLE (65862-829-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/596c923d-db8d-4b96-bf31-52186a38c30d

  • NADAC price for package 65862082930

    GET /v1/drugs/nadac/65862082930

Use it

Look up 65862-829 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-829 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-829. 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.