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Tadalafil

NDC 72789-408, Tadalafil, tablet, film coated, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-408
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
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/72789-408 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TADALAFIL10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72789-408-307278904083030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-408-30)
72789-408-907278904089090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-408-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/828f0ee1-b9fc-4743-9394-fc086bcf5345

Use it

Look up 72789-408 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-408 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-408. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.