Tadalafil
NDC 72789-408, Tadalafil, tablet, film coated, from PD-Rx Pharmaceuticals, Inc..
- Product NDC
- 72789-408
- Status
- Listed
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA211298
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72789-408 \ -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 NDC | NDC-11 | Package |
|---|---|---|
| 72789-408-30 | 72789040830 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-408-30) |
| 72789-408-90 | 72789040890 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-408-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/828f0ee1-b9fc-4743-9394-fc086bcf5345
Use it
Look up 72789-408 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72789-408 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72789-408. 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.