Terbinafine Hydrochloride
NDC 43353-893, Terbinafine Hydrochloride, tablet, from Aphena Pharma Solutions - Tennessee, LLC.
- Product NDC
- 43353-893
- Status
- Listed
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- 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/43353-893 \ -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 |
|---|---|---|
| 43353-893-16 | 43353089316 | 6000 TABLET in 1 BOTTLE (43353-893-16) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/808dab18-43f1-4895-a023-edbde722863e
Use it
Look up 43353-893 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/43353-893 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 43353-893. 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.