NDC product
JBA Joint Revive The Legend I
NDC 13411-859 · Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals
Key facts
| Product NDC | 13411-859 |
|---|---|
| Proprietary name | JBA Joint Revive The Legend I |
| Nonproprietary name | Glucosamine Sulfate Potassium Chloride, Fucoidan Extract, Eggshell Membrane Collagen |
| Substances | LAMINARIA JAPONICA, EGG SHELL MEMBRANE, GLUCOSAMINE SULFATE POTASSIUM CHLORIDE |
| Dosage form | CAPSULE |
| Route | ORAL |
| Labeler | Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | Oct 28, 2024 |
| 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: