NDC product
Bepotastine Besilate
NDC 24208-630 · Bausch & Lomb Incorporated
Key facts
| Product NDC | 24208-630 |
|---|---|
| Proprietary name | Bepotastine Besilate |
| Nonproprietary name | bepotastine besilate |
| Substances | BEPOTASTINE BESILATE |
| Dosage form | SOLUTION/ DROPS |
| Route | OPHTHALMIC |
| Labeler | Bausch & Lomb Incorporated |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA AUTHORIZED GENERIC |
| Application number | NDA022288 |
| Pharmacologic classes | Histamine-1 Receptor Antagonist [EPC] |
| Marketing start | May 28, 2021 |
| 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: