NDC product
Sambucus comp.
NDC 48951-8435 · Uriel Pharmacy, Inc
Key facts
| Product NDC | 48951-8435 |
|---|---|
| Proprietary name | Sambucus comp. |
| Nonproprietary name | Sambucus comp. |
| Substances | SAMBUCUS NIGRA FLOWERING TOP, TEUCRIUM SCORODONIA WHOLE, BERBERIS VULGARIS ROOT BARK, PHOSPHORUS |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Uriel Pharmacy, Inc |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Sep 1, 2009 |
| 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: