Vardenafil Hydrochloride
NDC 0093-7654, Vardenafil Hydrochloride, tablet, film coated, from Teva Pharmaceuticals USA, Inc..
- Product NDC
- 0093-7654
- Status
- Listed
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA091347
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0093-7654 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- VARDENAFIL HYDROCHLORIDE10 mg/1
Pharmacologic classes
Phosphodiesterase 5 Inhibitor [EPC]; Phosphodiesterase 5 Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0093-7654-56 | 00093765456 | 30 TABLET, FILM COATED in 1 BOTTLE (0093-7654-56) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/e593ab58-70a4-4095-8091-16a4b6d49e4dNADAC price for package 00093765456
GET /v1/drugs/nadac/00093765456
Use it
Look up 0093-7654 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0093-7654 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0093-7654. 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.