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Selexipag

NDC 70710-1551, Selexipag, tablet, film coated, from Zydus Pharmaceuticals (USA) Inc..

Product NDC
70710-1551
Status
Listed
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214302
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1551 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SELEXIPAG200 ug/1

Pharmacologic classes

Prostacyclin Receptor Agonist [EPC]; Prostacyclin Receptor Agonists [MoA]

Package NDCNDC-11Package
70710-1551-67071015510660 TABLET, FILM COATED in 1 BOTTLE (70710-1551-6)
70710-1551-870710155108140 TABLET, FILM COATED in 1 BOTTLE (70710-1551-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c604e181-e336-4194-bf96-f65dd164d461

Use it

Look up 70710-1551 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1551 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1551. 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.