Data / Drug companies / Afaxys Pharma, LLC
Afaxys Pharma, LLC: 11 products in the FDA NDC directory, labeler code 50102
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Afaxys Pharma, LLC (labeler code 50102) lists 11 products in the FDA National Drug Code Directory, covering 6 finished drugs by generic name. By type: 10 prescription drugs, 1 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on February 27, 2018.
The request: Watch Afaxys Pharma, LLC (FDA labeler code 50102): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 50102
- Products in commercial distribution
- 11
- Packages
- 13
- Finished drugs by generic name
- 6
- Prescription products
- 10
- Over the counter products
- 1
- Flagged as original packager
- 11 of 11 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- July 6, 2016
- 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) | 11 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 10 | 90.9% |
| Over the counter drugs | 1 | 9.1% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Norgestimate and ethinyl estradiol | 3 | 20 |
| Levonorgestrel and ethinyl estradiol | 2 | 19 |
| Norethindrone | 1 | 17 |
| Drospirenone and ethinyl estradiol | 1 | 16 |
| Levonorgestrel | 1 | 31 |
| Desogestrel and ethinyl estradiol | 1 | 12 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Kit | 9 | 81.8% |
| Tablet | 2 | 18.2% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Progestin | 2 |
| Progestin-containing Intrauterine System | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Jasmiel | 50102-240 | Kit | Generic drugs (ANDA) | February 27, 2018 |
| EContra One-Step | 50102-211 | Tablet | Generic drugs (ANDA) | February 8, 2018 |
| Tarina Fe 1/20 EQ | 50102-228 | Kit | Generic drugs (ANDA) | June 16, 2017 |
| Tarina 24 fe | 50102-224 | Kit | Generic drugs (ANDA) | June 15, 2017 |
| Cyred EQ | 50102-254 | Kit | Generic drugs (ANDA) | May 17, 2017 |
| Aubra EQ | 50102-220 | Kit | Generic drugs (ANDA) | November 14, 2016 |
| Tri-VyLibra Lo | 50102-231 | Kit | Generic drugs (ANDA) | November 4, 2016 |
| Lyleq | 50102-300 | Tablet | Generic drugs (ANDA) | September 23, 2016 |
| Chateal EQ | 50102-230 | Kit | Generic drugs (ANDA) | September 23, 2016 |
| VyLibra | 50102-235 | Kit | Generic drugs (ANDA) | July 7, 2016 |
| Tri-VyLibra | 50102-233 | Kit | Generic drugs (ANDA) | July 6, 2016 |
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.