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Tadalafil

NDC 65862-852, Tadalafil, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
65862-852
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206285
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-852 \
  -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
65862-852-0565862085205500 TABLET, FILM COATED in 1 BOTTLE (65862-852-05)
65862-852-306586208523030 TABLET, FILM COATED in 1 BOTTLE (65862-852-30)
65862-852-99658620852991000 TABLET, FILM COATED in 1 BOTTLE (65862-852-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0345b81b-f946-4dd6-b49d-2a2bdd4c49c9

Use it

Look up 65862-852 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-852 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-852. 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.