Data / Drug companies / Cycle Pharmaceuticals Ltd
Cycle Pharmaceuticals Ltd: 19 products in the FDA NDC directory, labeler code 70709
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Cycle Pharmaceuticals Ltd (labeler code 70709) lists 19 products in the FDA National Drug Code Directory, covering 8 finished drugs by generic name. By type: 19 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on June 30, 2026.
The request: Watch Cycle Pharmaceuticals Ltd (FDA labeler code 70709): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 70709
- Products in commercial distribution
- 19
- Packages
- 20
- Finished drugs by generic name
- 8
- Prescription products
- 19
- Over the counter products
- 0
- Flagged as original packager
- 8 of 8 products that carry the flag
- Started marketing in the last 12 months
- 2
- Earliest marketing start
- July 26, 2017
- 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) | 14 | 73.7% |
| Generic drugs (ANDA) | 5 | 26.3% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 19 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Dasatinib | 6 | 18 |
| Nitisinone | 4 | 6 |
| Nilotinib | 2 | 10 |
| Tiopronin | 2 | 8 |
| Fingolimod lauryl sulfate | 2 | 1 |
| Penicillamine | 1 | 12 |
| Icatibant | 1 | 8 |
| Dichlorphenamide | 1 | 4 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 11 | 57.9% |
| Tablet, orally disintegrating | 4 | 21.1% |
| Tablet, delayed release | 2 | 10.5% |
| Capsule | 1 | 5.3% |
| Injection | 1 | 5.3% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Cavhanza | 70709-192 | Tablet, orally disintegrating | New drug applications (NDA) | June 30, 2026 |
| Cavhanza | 70709-191 | Tablet, orally disintegrating | New drug applications (NDA) | June 30, 2026 |
| Aagylur | 70709-102 | Capsule | Generic drugs (ANDA) | September 25, 2025 |
| Phyrago | 70709-156 | Tablet | New drug applications (NDA) | September 22, 2025 |
| Phyrago | 70709-155 | Tablet | New drug applications (NDA) | September 22, 2025 |
| Phyrago | 70709-154 | Tablet | New drug applications (NDA) | September 22, 2025 |
| Phyrago | 70709-153 | Tablet | New drug applications (NDA) | September 22, 2025 |
| Phyrago | 70709-152 | Tablet | New drug applications (NDA) | September 22, 2025 |
| Phyrago | 70709-151 | Tablet | New drug applications (NDA) | September 22, 2025 |
| Harliku | 70709-112 | Tablet | New drug applications (NDA) | July 21, 2025 |
| Venxxiva | 70709-123 | Tablet, delayed release | Generic drugs (ANDA) | January 22, 2025 |
| Venxxiva | 70709-121 | Tablet, delayed release | Generic drugs (ANDA) | January 22, 2025 |
| Ormalvi | 70709-085 | Tablet | Generic drugs (ANDA) | March 15, 2024 |
| Tascenso odt | 70709-065 | Tablet, orally disintegrating | New drug applications (NDA) | February 1, 2023 |
| Tascenso odt | 70709-062 | Tablet, orally disintegrating | New drug applications (NDA) | February 1, 2023 |
| Sajazir | 70709-013 | Injection | Generic drugs (ANDA) | June 3, 2021 |
| Nityr | 70709-005 | Tablet | New drug applications (NDA) | July 26, 2017 |
| Nityr | 70709-002 | Tablet | New drug applications (NDA) | July 26, 2017 |
| Nityr | 70709-000 | Tablet | New drug applications (NDA) | July 26, 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.