Terbinafine Hydrochloride
NDC 50090-1048, Terbinafine Hydrochloride, tablet, from A-S Medication Solutions.
- Product NDC
- 50090-1048
- Status
- Listed
- Labeler
- A-S Medication Solutions
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA077714
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50090-1048 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- TERBINAFINE HYDROCHLORIDE250 mg/1
Pharmacologic classes
Allylamine Antifungal [EPC]; Allylamine [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 50090-1048-0 | 50090104800 | 30 TABLET in 1 BOTTLE (50090-1048-0) |
| 50090-1048-1 | 50090104801 | 90 TABLET in 1 BOTTLE (50090-1048-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/6605103b-fd71-4438-8496-f48973b98901
Use it
Look up 50090-1048 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50090-1048 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50090-1048. 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.