Data / Drug companies / Bostal LLC
Bostal LLC: 22 products in the FDA NDC directory, labeler code 35561
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Bostal LLC (labeler code 35561) lists 22 products in the FDA National Drug Code Directory, covering 7 finished drugs by generic name. By type: 22 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on July 16, 2022.
The request: Watch Bostal LLC (FDA labeler code 35561): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 35561
- Products in commercial distribution
- 22
- Packages
- 60
- Finished drugs by generic name
- 7
- Prescription products
- 22
- Over the counter products
- 0
- Flagged as original packager
- 22 of 22 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- November 17, 2017
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 22 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 22 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Fenofibrate | 7 | 56 |
| Tadalafil | 4 | 54 |
| Sildenafil | 3 | 53 |
| Carbamazepine | 3 | 52 |
| Methocarbamol | 3 | 67 |
| Solifenacin succiate | 1 | 2 |
| Solifenacin succinate | 1 | 22 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 13 | 59.1% |
| Capsule | 3 | 13.6% |
| Tablet, extended release | 3 | 13.6% |
| Tablet, coated | 3 | 13.6% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Peroxisome Proliferator Receptor alpha Agonist | 7 |
| Phosphodiesterase 5 Inhibitor | 7 |
| Mood Stabilizer | 3 |
| Muscle Relaxant | 3 |
| Cholinergic Muscarinic Antagonist | 2 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Methocarbamol | 35561-349 | Tablet, coated | Generic drugs (ANDA) | July 16, 2022 |
| Carbamazepine er | 35561-357 | Tablet, extended release | Generic drugs (ANDA) | March 31, 2022 |
| Carbamazepine er | 35561-356 | Tablet, extended release | Generic drugs (ANDA) | March 31, 2022 |
| Carbamazepine er | 35561-355 | Tablet, extended release | Generic drugs (ANDA) | March 31, 2022 |
| Fenofibrate | 35561-250 | Tablet, film coated | Generic drugs (ANDA) | January 1, 2021 |
| Fenofibrate | 35561-249 | Tablet, film coated | Generic drugs (ANDA) | January 1, 2021 |
| Sildenafil | 35561-253 | Tablet, film coated | Generic drugs (ANDA) | April 22, 2020 |
| Sildenafil | 35561-252 | Tablet, film coated | Generic drugs (ANDA) | April 22, 2020 |
| Sildenafil | 35561-251 | Tablet, film coated | Generic drugs (ANDA) | April 22, 2020 |
| Tadalafil | 35561-257 | Tablet, film coated | Generic drugs (ANDA) | November 29, 2019 |
| Tadalafil | 35561-256 | Tablet, film coated | Generic drugs (ANDA) | November 29, 2019 |
| Tadalafil | 35561-255 | Tablet, film coated | Generic drugs (ANDA) | November 29, 2019 |
| Tadalafil | 35561-254 | Tablet, film coated | Generic drugs (ANDA) | November 29, 2019 |
| Fenofibrate | 35561-344 | Tablet, film coated | Generic drugs (ANDA) | June 30, 2019 |
| Fenofibrate | 35561-343 | Tablet, film coated | Generic drugs (ANDA) | June 30, 2019 |
| Solifenacin Succinate | 35561-286 | Tablet, film coated | Generic drugs (ANDA) | May 20, 2019 |
| Solifenacin Succinate | 35561-285 | Tablet, film coated | Generic drugs (ANDA) | May 20, 2019 |
| Methocarbamol | 35561-212 | Tablet, coated | Generic drugs (ANDA) | October 10, 2018 |
| Methocarbamol | 35561-211 | Tablet, coated | Generic drugs (ANDA) | October 9, 2018 |
| Fenofibrate | 35561-347 | Capsule | Generic drugs (ANDA) | November 17, 2017 |
| Fenofibrate | 35561-346 | Capsule | Generic drugs (ANDA) | November 17, 2017 |
| Fenofibrate | 35561-345 | Capsule | Generic drugs (ANDA) | November 17, 2017 |
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.