Sildenafil
NDC 72303-0846, Sildenafil, tablet, film coated, from HEC Pharm USA Inc..
- Product NDC
- 72303-0846
- Status
- Listed
- Labeler
- HEC Pharm USA Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA213032
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72303-0846 \ -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 |
|---|---|---|
| 72303-0846-1 | 72303084601 | 30 TABLET, FILM COATED in 1 BOTTLE (72303-0846-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/4c57d855-3b49-fe6e-e063-6294a90a5cd5
Use it
Look up 72303-0846 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72303-0846 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72303-0846. 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.