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Tadalafil

NDC 47335-012, Tadalafil, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-012
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208934
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-012 \
  -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
47335-012-834733500128330 TABLET, FILM COATED in 1 BOTTLE (47335-012-83)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/168a135b-1454-4def-9b03-c9a470bfcb5f

Use it

Look up 47335-012 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-012 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-012. 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.