NDC product
Hyosyne
NDC 54838-511 · Lannett Company, Inc.
Key facts
| Product NDC | 54838-511 |
|---|---|
| Proprietary name | Hyosyne |
| Nonproprietary name | Hyoscyamine Sulfate |
| Substances | HYOSCYAMINE SULFATE |
| Dosage form | ELIXIR |
| Route | ORAL |
| Labeler | Lannett Company, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | Nov 1, 1997 |
| 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: