NDC product
Methylprednisolone Sodium Succinate
NDC 70121-1001 · Amneal Pharmaceuticals LLC
Key facts
| Product NDC | 70121-1001 |
|---|---|
| Proprietary name | Methylprednisolone Sodium Succinate |
| Nonproprietary name | Methylprednisolone |
| Substances | METHYLPREDNISOLONE SODIUM SUCCINATE |
| Dosage form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route | INTRAMUSCULAR, INTRAVENOUS |
| Labeler | Amneal Pharmaceuticals LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA207549 |
| Pharmacologic classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
| Marketing start | Nov 11, 2016 |
| 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: