Tadalafil
NDC 43598-578, Tadalafil, tablet, film coated, from Dr.Reddys Laboratories Inc.
- Product NDC
- 43598-578
- Status
- Listed
- Labeler
- Dr.Reddys Laboratories Inc
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210145
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/43598-578 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- TADALAFIL20 mg/1
Pharmacologic classes
Phosphodiesterase 5 Inhibitor [EPC]; Phosphodiesterase 5 Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 43598-578-30 | 43598057830 | 30 TABLET, FILM COATED in 1 BOTTLE (43598-578-30) |
| 43598-578-60 | 43598057860 | 60 TABLET, FILM COATED in 1 BOTTLE (43598-578-60) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/61955171-ca57-e300-1983-9472a56ca976NADAC price for package 43598057860
GET /v1/drugs/nadac/43598057860
Use it
Look up 43598-578 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/43598-578 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 43598-578. 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.