NDC product
PROSCENAT
NDC 59469-314 · PEKANA Naturheilmittel GmbH
Key facts
| Product NDC | 59469-314 |
|---|---|
| Proprietary name | PROSCENAT |
| Nonproprietary name | SULFURIC ACID, Lytta vesicatoria, Conium maculatum Flowering Top, Selenium, Delphinium staphisagria Seed, Nasturtium officinale Whole, and Ononis spinosa Whole |
| Substances | SULFURIC ACID, LYTTA VESICATORIA, CONIUM MACULATUM FLOWERING TOP, SELENIUM, DELPHINIUM STAPHISAGRIA SEED, NASTURTIUM OFFICINALE WHOLE, ONONIS SPINOSA WHOLE |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | PEKANA Naturheilmittel GmbH |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Jun 24, 2019 |
| 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: