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Sildenafil

NDC 71209-108, Sildenafil, tablet, film coated, from Cadila Pharmaceuticals Limited.

Product NDC
71209-108
Status
Listed
Labeler
Cadila Pharmaceuticals Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218045
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71209-108 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SILDENAFIL CITRATE100 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71209-108-017120901080130 TABLET, FILM COATED in 1 BOTTLE (71209-108-01)
71209-108-0571209010805100 TABLET, FILM COATED in 1 BOTTLE (71209-108-05)
71209-108-11712090108111000 TABLET, FILM COATED in 1 BOTTLE (71209-108-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c079fc41-7b9a-499d-88ea-86ccb65c828d

Use it

Look up 71209-108 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71209-108 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71209-108. 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.