NDC product
PRED FORTE
NDC 11980-180 · Allergan, Inc.
Key facts
| Product NDC | 11980-180 |
|---|---|
| Proprietary name | PRED FORTE |
| Nonproprietary name | prednisolone acetate |
| Substances | PREDNISOLONE ACETATE |
| Dosage form | SUSPENSION/ DROPS |
| Route | OPHTHALMIC |
| Labeler | Allergan, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Application number | NDA017011 |
| Pharmacologic classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
| Marketing start | Jun 1, 1973 |
| Marketing end | May 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