NDC product
TERBINAFINE HYDROCHLORIDE
NDC 69292-225 · Amici Pharma, Inc.
Key facts
| Product NDC | 69292-225 |
|---|---|
| Proprietary name | TERBINAFINE HYDROCHLORIDE |
| Nonproprietary name | Terbinafine Tablets 250 mg |
| Substances | TERBINAFINE HYDROCHLORIDE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Amici Pharma, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA076390 |
| Pharmacologic classes | Allylamine Antifungal [EPC], Allylamine [CS] |
| Marketing start | Feb 18, 2026 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: