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Tadalafil

NDC 60290-027, Tadalafil, tablet, film coated, from Umedica Laboratories USA Inc..

Product NDC
60290-027
Status
Listed
Labeler
Umedica Laboratories USA 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/60290-027 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TADALAFIL2.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
60290-027-016029000270130 TABLET, FILM COATED in 1 BOTTLE (60290-027-01)
60290-027-02602900027021000 TABLET, FILM COATED in 1 BOTTLE (60290-027-02)
60290-027-036029000270330 TABLET, FILM COATED in 1 BLISTER PACK (60290-027-03)
60290-027-0460290002704500 TABLET, FILM COATED in 1 BOTTLE (60290-027-04)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6caf3b55-9bf4-4355-9e25-8bf368943fdd

Use it

Look up 60290-027 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60290-027 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60290-027. 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.