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Sildenafil

NDC 72789-098, Sildenafil, tablet, film coated, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-098
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202659
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72789-098 \
  -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
72789-098-107278900981010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-098-10)
72789-098-157278900981515 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-098-15)
72789-098-907278900989090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-098-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e1af7b6a-378e-4337-858f-85a926eec102

Use it

Look up 72789-098 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-098 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-098. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.