NDC product
JBA Joint Revive
NDC 13411-856 · Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals
Key facts
| Product NDC | 13411-856 |
|---|---|
| Proprietary name | JBA Joint Revive |
| Nonproprietary name | Glucosamine Sulfate Potassium Chloride, White Willow Bark Extract, Eggshell Membrane Collagen, Chondroitin Sulfate, Turmeric Root Extract, Bromelain, Soy Lecithin |
| Substances | SALIX ALBA BARK, GLUCOSAMINE SULFATE POTASSIUM CHLORIDE, EGG SHELL MEMBRANE, CHONDROITIN SULFATE (BOVINE), TURMERIC, STEM BROMELAIN, SOYBEAN LECITHIN |
| 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 | Aug 13, 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: