NDC product
CAPSULE, EXTENDED RELEASE · Catalent Pharma Solutions, LLC
NDC 11014-0720 · Catalent Pharma Solutions, LLC
Key facts
| Product NDC | 11014-0720 |
|---|---|
| Nonproprietary name | DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE, AMPHETAMINE SULFATE |
| Substances | DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, AMPHETAMINE SULFATE, DEXTROAMPHETAMINE SULFATE |
| Dosage form | CAPSULE, EXTENDED RELEASE |
| Labeler | Catalent Pharma Solutions, LLC |
| Product type | DRUG FOR FURTHER PROCESSING |
| Marketing category | DRUG FOR FURTHER PROCESSING |
| DEA schedule | CII |
| Marketing start | Apr 20, 2024 |
| 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: