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Tadalafil

NDC 72603-782, Tadalafil, tablet, film coated, from NorthStar Rx, LLC.

Product NDC
72603-782
Status
Listed
Labeler
NorthStar Rx, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211298
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72603-782 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TADALAFIL5 mg/1

Pharmacologic classes

Phosphodiesterase 5 Inhibitor [EPC]; Phosphodiesterase 5 Inhibitors [MoA]

Package NDCNDC-11Package
72603-782-01726030782011000 TABLET, FILM COATED in 1 BOTTLE (72603-782-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a10d464a-6ea7-4e5a-befa-71eceacc5039

Use it

Look up 72603-782 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72603-782 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72603-782. 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.