Data / Drug companies / Amneal Pharmaceuticals LLC
Amneal Pharmaceuticals LLC: 20 products in the FDA NDC directory, labeler code 60846
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Amneal Pharmaceuticals LLC (labeler code 60846) lists 20 products in the FDA National Drug Code Directory, covering 6 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 October 9, 2024.
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- Labeler code
- 60846
- Products in commercial distribution
- 20
- Packages
- 20
- Finished drugs by generic name
- 6
- Prescription products
- 20
- Over the counter products
- 0
- Flagged as original packager
- 20 of 20 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- January 1, 2014
- 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) | 15 | 75% |
| Generic drugs (ANDA) | 3 | 15% |
| Other unapproved drugs | 2 | 10% |
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 |
|---|---|---|
| Levothyroxine sodium | 12 | 44 |
| Zolmitriptan | 2 | 22 |
| Estradiol/norethindrone acetate | 2 | 2 |
| Phenazopyridine | 2 | 13 |
| Pyridostigmine bromide | 1 | 20 |
| Nizatidine | 1 | 4 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 12 | 60% |
| Tablet, film coated | 6 | 30% |
| Tablet, extended release | 1 | 5% |
| Solution | 1 | 5% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| l-Thyroxine | 12 |
| Serotonin-1b and Serotonin-1d Receptor Agonist | 2 |
| Estrogen | 2 |
| Progestin | 2 |
| Cholinesterase Inhibitor | 1 |
| Histamine-2 Receptor Antagonist | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Pyridostigmine bromide | 60846-559 | Tablet, extended release | New drug applications (NDA) | October 9, 2024 |
| Zomig | 60846-133 | Tablet, film coated | Generic drugs (ANDA) | January 9, 2023 |
| Zomig | 60846-130 | Tablet, film coated | Generic drugs (ANDA) | January 9, 2023 |
| Activella | 60846-232 | Tablet, film coated | New drug applications (NDA) | May 1, 2019 |
| Activella | 60846-231 | Tablet, film coated | New drug applications (NDA) | May 1, 2019 |
| Nizatidine | 60846-301 | Solution | Generic drugs (ANDA) | August 12, 2016 |
| Unithroid | 60846-812 | Tablet | New drug applications (NDA) | July 3, 2014 |
| Unithroid | 60846-811 | Tablet | New drug applications (NDA) | July 3, 2014 |
| Unithroid | 60846-810 | Tablet | New drug applications (NDA) | July 3, 2014 |
| Unithroid | 60846-809 | Tablet | New drug applications (NDA) | July 3, 2014 |
| Unithroid | 60846-808 | Tablet | New drug applications (NDA) | July 3, 2014 |
| Unithroid | 60846-807 | Tablet | New drug applications (NDA) | July 3, 2014 |
| Unithroid | 60846-806 | Tablet | New drug applications (NDA) | July 3, 2014 |
| Unithroid | 60846-805 | Tablet | New drug applications (NDA) | July 3, 2014 |
| Unithroid | 60846-804 | Tablet | New drug applications (NDA) | July 3, 2014 |
| Unithroid | 60846-803 | Tablet | New drug applications (NDA) | July 3, 2014 |
| Unithroid | 60846-802 | Tablet | New drug applications (NDA) | July 3, 2014 |
| Unithroid | 60846-801 | Tablet | New drug applications (NDA) | July 3, 2014 |
| Pyridium | 60846-502 | Tablet, film coated | Other unapproved drugs | January 1, 2014 |
| Pyridium | 60846-501 | Tablet, film coated | Other unapproved drugs | January 1, 2014 |
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.