Data / Drug companies / Bausch & Lomb Americas Inc.
Bausch & Lomb Americas Inc.: 18 products in the FDA NDC directory, labeler code 82260
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Bausch & Lomb Americas Inc. (labeler code 82260) lists 18 products in the FDA National Drug Code Directory, covering 10 finished drugs by generic name. By type: 18 prescription drugs. Its main marketing category is authorized generics (NDA). The newest product started marketing on January 9, 2026.
The request: Watch Bausch & Lomb Americas Inc. (FDA labeler code 82260): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 82260
- Products in commercial distribution
- 18
- Packages
- 26
- Finished drugs by generic name
- 10
- Prescription products
- 18
- Over the counter products
- 0
- Flagged as original packager
- 18 of 18 products that carry the flag
- Started marketing in the last 12 months
- 2
- Earliest marketing start
- February 14, 2018
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Authorized generics (NDA) | 17 | 94.4% |
| New drug applications (NDA) | 1 | 5.6% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 18 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Solution/ drops | 8 | 44.4% |
| Solution | 6 | 33.3% |
| Suspension/ drops | 2 | 11.1% |
| Suspension | 1 | 5.6% |
| Gel | 1 | 5.6% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Besivance | 82260-466 | Suspension | New drug applications (NDA) | January 9, 2026 |
| Loteprednol etabonate and tobramycin | 82260-358 | Solution/ drops | Authorized generics (NDA) | January 9, 2026 |
| Loteprednol etabonate | 82260-361 | Suspension/ drops | Authorized generics (NDA) | February 9, 2024 |
| Bromfenac ophthalmic solution | 82260-602 | Solution/ drops | Authorized generics (NDA) | January 8, 2024 |
| Loteprednol Etabonate | 82260-508 | Gel | Authorized generics (NDA) | June 30, 2023 |
| Atropine Sulfate | 82260-001 | Solution | Authorized generics (NDA) | April 21, 2023 |
| Loteprednol Etabonate | 82260-299 | Suspension/ drops | Authorized generics (NDA) | April 7, 2023 |
| Phenylephrine Hydrochloride | 82260-103 | Solution/ drops | Authorized generics (NDA) | March 31, 2023 |
| Phenylephrine Hydrochloride | 82260-102 | Solution/ drops | Authorized generics (NDA) | March 31, 2023 |
| Tetracaine Hydrochloride | 82260-920 | Solution/ drops | Authorized generics (NDA) | September 21, 2022 |
| Timolol Maleate | 82260-045 | Solution/ drops | Authorized generics (NDA) | June 23, 2022 |
| Timolol Maleate | 82260-496 | Solution | Authorized generics (NDA) | February 17, 2022 |
| Bepotastine Besilate | 82260-630 | Solution/ drops | Authorized generics (NDA) | May 28, 2021 |
| Timolol Maleate | 82260-813 | Solution | Authorized generics (NDA) | June 1, 2020 |
| Timolol Maleate | 82260-812 | Solution | Authorized generics (NDA) | June 1, 2020 |
| Fluorescein Sodium and Benoxinate Hydrochloride | 82260-734 | Solution/ drops | Authorized generics (NDA) | March 20, 2020 |
| Timolol Maleate | 82260-819 | Solution | Authorized generics (NDA) | February 14, 2018 |
| Timolol Maleate | 82260-818 | Solution | Authorized generics (NDA) | February 14, 2018 |
CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.