NDC product
POWDER · Avantor Performance Materials, LLC
NDC 10106-3802 · Avantor Performance Materials, LLC
Key facts
| Product NDC | 10106-3802 |
|---|---|
| Nonproprietary name | SODIUM PHOSPHATE MONOBASIC MONOHYDRATE |
| Substances | SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE |
| Dosage form | POWDER |
| Labeler | Avantor Performance Materials, LLC |
| Product type | BULK INGREDIENT |
| Marketing category | BULK INGREDIENT |
| Marketing start | Feb 13, 2008 |
| Listing certified through | Dec 31, 2027 |
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: