NDC product
POWDER · SpecGx LLC
NDC 0406-1592 · SpecGx LLC
Key facts
| Product NDC | 0406-1592 |
|---|---|
| Nonproprietary name | Diphenoxylate Hydrochloride |
| Substances | DIPHENOXYLATE HYDROCHLORIDE |
| Dosage form | POWDER |
| Labeler | SpecGx LLC |
| Product type | BULK INGREDIENT |
| Marketing category | BULK INGREDIENT |
| DEA schedule | CII |
| Marketing start | Nov 21, 2013 |
| 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: