Tadalafil
NDC 65862-851, Tadalafil, tablet, film coated, from Aurobindo Pharma Limited.
- Product NDC
- 65862-851
- Status
- Listed
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA206285
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/65862-851 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- TADALAFIL5 mg/1
Pharmacologic classes
Phosphodiesterase 5 Inhibitor [EPC]; Phosphodiesterase 5 Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 65862-851-30 | 65862085130 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-851-30) |
| 65862-851-32 | 65862085132 | 2 BLISTER PACK in 1 CARTON (65862-851-32) / 15 TABLET, FILM COATED in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/0345b81b-f946-4dd6-b49d-2a2bdd4c49c9
Use it
Look up 65862-851 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/65862-851 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 65862-851. 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.