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Prasugrel

NDC 29300-302, Prasugrel, tablet, film coated, from Unichem Pharmaceuticals (USA), Inc..

Product NDC
29300-302
Status
Listed
Labeler
Unichem Pharmaceuticals (USA), Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213315
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/29300-302 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRASUGREL HYDROCHLORIDE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
29300-302-132930003021330 TABLET, FILM COATED in 1 BOTTLE (29300-302-13)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5edc1ab3-5c7a-47d6-8aaa-00523c9b4c8f

  • NADAC price for package 29300030213

    GET /v1/drugs/nadac/29300030213

Use it

Look up 29300-302 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/29300-302 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 29300-302. 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.