NDC product
PATADAY ONCE DAILY RELIEF
NDC 0065-8150 · Alcon Laboratories, Inc.
Key facts
| Product NDC | 0065-8150 |
|---|---|
| Proprietary name | PATADAY ONCE DAILY RELIEF |
| Nonproprietary name | OLOPATADINE HYDROCHLORIDE |
| Substances | OLOPATADINE HYDROCHLORIDE |
| Dosage form | SOLUTION |
| Route | OPHTHALMIC |
| Labeler | Alcon Laboratories, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | NDA |
| Application number | NDA021545 |
| Pharmacologic classes | Decreased Histamine Release [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Histamine-1 Receptor Inhibitor [EPC], Mast Cell Stabilizer [EPC] |
| Marketing start | Feb 28, 2020 |
| 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: