Data / Drug companies / Knoa Pharma LLC
Knoa Pharma LLC: 20 products in the FDA NDC directory, labeler code 59011
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Knoa Pharma LLC (labeler code 59011) lists 20 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 20 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on August 7, 2025.
The request: Watch Knoa Pharma LLC (FDA labeler code 59011): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 59011
- Products in commercial distribution
- 20
- Packages
- 27
- Finished drugs by generic name
- 4
- Prescription products
- 20
- Over the counter products
- 0
- Controlled substance products
- Schedule II 13, Schedule III 5
- Flagged as original packager
- 20 of 20 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- August 8, 2010
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| New drug applications (NDA) | 19 | 95% |
| Generic drugs (ANDA) | 1 | 5% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 20 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Oxycodone hydrochloride | 7 | 36 |
| Hydrocodone bitartrate | 6 | 2 |
| Buprenorphine | 5 | 24 |
| Nalmefene hydrochloride | 2 | 2 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated, extended release | 7 | 35% |
| Tablet, extended release | 6 | 30% |
| Patch, extended release | 5 | 25% |
| Injection, solution | 2 | 10% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Opioid Agonist | 13 |
| Partial Opioid Agonist | 5 |
| Opioid Antagonist | 2 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Zurnai | 59011-962 | Injection, solution | New drug applications (NDA) | August 7, 2025 |
| Nalmefene hydrochloride | 59011-960 | Injection, solution | Generic drugs (ANDA) | February 8, 2022 |
| Hysingla ER | 59011-276 | Tablet, extended release | New drug applications (NDA) | January 15, 2015 |
| Hysingla ER | 59011-275 | Tablet, extended release | New drug applications (NDA) | January 15, 2015 |
| Hysingla ER | 59011-274 | Tablet, extended release | New drug applications (NDA) | January 15, 2015 |
| Hysingla ER | 59011-273 | Tablet, extended release | New drug applications (NDA) | January 15, 2015 |
| Hysingla ER | 59011-272 | Tablet, extended release | New drug applications (NDA) | January 15, 2015 |
| Hysingla ER | 59011-271 | Tablet, extended release | New drug applications (NDA) | January 15, 2015 |
| Butrans | 59011-758 | Patch, extended release | New drug applications (NDA) | February 14, 2011 |
| Butrans | 59011-757 | Patch, extended release | New drug applications (NDA) | February 14, 2011 |
| Butrans | 59011-752 | Patch, extended release | New drug applications (NDA) | February 14, 2011 |
| Butrans | 59011-751 | Patch, extended release | New drug applications (NDA) | February 14, 2011 |
| Butrans | 59011-750 | Patch, extended release | New drug applications (NDA) | February 14, 2011 |
| OxyContin | 59011-480 | Tablet, film coated, extended release | New drug applications (NDA) | August 8, 2010 |
| OxyContin | 59011-460 | Tablet, film coated, extended release | New drug applications (NDA) | August 8, 2010 |
| OxyContin | 59011-440 | Tablet, film coated, extended release | New drug applications (NDA) | August 8, 2010 |
| OxyContin | 59011-430 | Tablet, film coated, extended release | New drug applications (NDA) | August 8, 2010 |
| OxyContin | 59011-420 | Tablet, film coated, extended release | New drug applications (NDA) | August 8, 2010 |
| OxyContin | 59011-415 | Tablet, film coated, extended release | New drug applications (NDA) | August 8, 2010 |
| OxyContin | 59011-410 | Tablet, film coated, extended release | New drug applications (NDA) | August 8, 2010 |
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.