NDC product
Arnica Montana
NDC 34666-091 · NARTEX LABORATORIOS HOMEOPATICOS SA DE CV
Key facts
| Product NDC | 34666-091 |
|---|---|
| Proprietary name | Arnica Montana |
| Nonproprietary name | Arnica Montana |
| Substances | ARNICA MONTANA |
| Dosage form | PELLET |
| Route | ORAL |
| Labeler | NARTEX LABORATORIOS HOMEOPATICOS SA DE CV |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | May 8, 2025 |
| Listing certified through | Dec 31, 2026 |
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: