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tadalafil

NDC 71821-009, Tadalafil, tablet, film coated, from VKT Pharma Private Limited.

Product NDC
71821-009
Status
Listed
Labeler
VKT Pharma Private Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215556
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71821-009 \
  -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
71821-009-017182100090130 TABLET, FILM COATED in 1 BOTTLE (71821-009-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b4d9851c-5c06-4532-bd82-16d92b60c28f

Use it

Look up 71821-009 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71821-009 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71821-009. 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.