NDC product
Borrelia Burgdorferi
NDC 55714-9001 · Newton Laboratories, Inc.
Key facts
| Product NDC | 55714-9001 |
|---|---|
| Proprietary name | Borrelia Burgdorferi |
| Nonproprietary name | Borrelia Burgdorferi |
| Substances | BORRELIA BURGDORFERI |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Newton Laboratories, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Jan 1, 2020 |
| 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: