NDC product
Oxymorphone hydrochloride
NDC 0115-1233 · Amneal Pharmaceuticals of New York LLC
Key facts
| Product NDC | 0115-1233 |
|---|---|
| Proprietary name | Oxymorphone hydrochloride |
| Nonproprietary name | Oxymorphone hydrochloride |
| Substances | OXYMORPHONE HYDROCHLORIDE |
| Dosage form | TABLET, FILM COATED, EXTENDED RELEASE |
| Route | ORAL |
| Labeler | Amneal Pharmaceuticals of New York LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA079087 |
| DEA schedule | CII |
| Pharmacologic classes | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
| Marketing start | Jan 2, 2013 |
| 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: