NDC product
POWDER · Kyowa Pharma Chemical Co., Ltd.
NDC 12079-2002 · Kyowa Pharma Chemical Co., Ltd.
Key facts
| Product NDC | 12079-2002 |
|---|---|
| Nonproprietary name | Olopatadine Hydrochloride |
| Substances | OLOPATADINE HYDROCHLORIDE |
| Dosage form | POWDER |
| Labeler | Kyowa Pharma Chemical Co., Ltd. |
| Product type | BULK INGREDIENT |
| Marketing category | BULK INGREDIENT |
| Marketing start | Oct 15, 2013 |
| Listing certified through | Dec 31, 2026 |
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: