SILDENAFIL CITRATE
NDC 71205-721, SILDENAFIL CITRATE, tablet, from Proficient Rx LP.
- Product NDC
- 71205-721
- Status
- Listed
- Labeler
- Proficient Rx LP
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209302
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71205-721 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SILDENAFIL CITRATE50 mg/1
Pharmacologic classes
Phosphodiesterase 5 Inhibitor [EPC]; Phosphodiesterase 5 Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71205-721-04 | 71205072104 | 4 TABLET in 1 BOTTLE (71205-721-04) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/59b623bc-fbdd-4f32-8327-0d600763f429
Use it
Look up 71205-721 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71205-721 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71205-721. 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.