NDC product
Clotrimazole Topical Solution USP, 1%
NDC 71297-030 · Allegis Holdings, LLC
Key facts
| Product NDC | 71297-030 |
|---|---|
| Proprietary name | Clotrimazole Topical Solution USP, 1% |
| Nonproprietary name | Clotrimazole Topical Solution USP, 1% |
| Substances | CLOTRIMAZOLE |
| Dosage form | SOLUTION |
| Route | TOPICAL |
| Labeler | Allegis Holdings, LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA216569 |
| Pharmacologic classes | Azole Antifungal [EPC], Azoles [CS] |
| Marketing start | Nov 12, 2025 |
| 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: