NDC product
Hyoscyamine Sulfate
NDC 16477-738 · Laser Pharmaceuticals, LLC
Key facts
| Product NDC | 16477-738 |
|---|---|
| Proprietary name | Hyoscyamine Sulfate |
| Nonproprietary name | Hyoscyamine Sulfate |
| Substances | HYOSCYAMINE SULFATE |
| Dosage form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Labeler | Laser Pharmaceuticals, LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | Jan 26, 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: