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Tadalafil

NDC 71205-720, Tadalafil, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-720
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209167
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-720 \
  -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
71205-720-04712050720044 TABLET, FILM COATED in 1 BOTTLE (71205-720-04)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7a105ef9-7129-4ce1-bd8d-ae316bf348e2

Use it

Look up 71205-720 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-720 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-720. 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.