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Tadalafil

NDC 71205-268, Tadalafil, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-268
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/71205-268 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TADALAFIL20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71205-268-107120502681010 TABLET, FILM COATED in 1 BOTTLE (71205-268-10)
71205-268-307120502683030 TABLET, FILM COATED in 1 BOTTLE (71205-268-30)
71205-268-607120502686060 TABLET, FILM COATED in 1 BOTTLE (71205-268-60)
71205-268-907120502689090 TABLET, FILM COATED in 1 BOTTLE (71205-268-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6fa9d4fa-86c9-4791-b28b-78e8b9341cea

Use it

Look up 71205-268 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-268 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-268. 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.