Data / Drug companies / Shenzhen Paxi Trading Co., Ltd.
Shenzhen Paxi Trading Co., Ltd.: 15 products in the FDA NDC directory, labeler code 85835
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Shenzhen Paxi Trading Co., Ltd. (labeler code 85835) lists 15 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 15 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on December 9, 2025.
The request: Watch Shenzhen Paxi Trading Co., Ltd. (FDA labeler code 85835): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 85835
- Products in commercial distribution
- 15
- Packages
- 19
- Finished drugs by generic name
- 5
- Prescription products
- 0
- Over the counter products
- 15
- Flagged as original packager
- 15 of 15 products that carry the flag
- Started marketing in the last 12 months
- 7
- Earliest marketing start
- June 30, 2025
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Over the counter monograph drugs | 15 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 15 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Nicotine transdermal patches | 8 | 2 |
| Nicotine patches | 4 | 4 |
| 21mg nicotine patches | 1 | 1 |
| 7mg nicotine patches | 1 | 1 |
| 14mg nicotine patches | 1 | 1 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Patch | 15 | 100% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Cholinergic Nicotinic Agonist | 15 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| WOFANLI Quit Smoking Nicotine Patches | 85835-016 | Patch | Over the counter monograph drugs | December 9, 2025 |
| NicDuic Quit Smoking Nicotine Patches 1-3 Step | 85835-015 | Patch | Over the counter monograph drugs | November 22, 2025 |
| NicDuic Quit Smoking Nicotine Patches 1-3 Step | 85835-014 | Patch | Over the counter monograph drugs | November 22, 2025 |
| NicDuic Quit Smoking Nicotine Patches 1-3 Step | 85835-013 | Patch | Over the counter monograph drugs | November 22, 2025 |
| NicDuic Quit Smoking Nicotine Patches 1 Step | 85835-012 | Patch | Over the counter monograph drugs | November 22, 2025 |
| NicDuic Quit Smoking Nicotine Patches 2 Step | 85835-011 | Patch | Over the counter monograph drugs | November 22, 2025 |
| NicDuic Quit Smoking Nicotine Patches 3 Step | 85835-010 | Patch | Over the counter monograph drugs | November 22, 2025 |
| WOFANLI Quit Smoking Nicotine Patches | 85835-009 | Patch | Over the counter monograph drugs | October 16, 2025 |
| WOFANLI Quit Smoking Nicotine Patches | 85835-008 | Patch | Over the counter monograph drugs | October 16, 2025 |
| WOFANLI Quit Smoking Nicotine Patches | 85835-007 | Patch | Over the counter monograph drugs | October 15, 2025 |
| WOFANLI Quit Smoking Nicotine Patches | 85835-006 | Patch | Over the counter monograph drugs | October 15, 2025 |
| WOFANLI Quit Smoking Nicotine Patches | 85835-005 | Patch | Over the counter monograph drugs | October 15, 2025 |
| WOFANLI Quit Smoking Nicotine Patches | 85835-004 | Patch | Over the counter monograph drugs | October 15, 2025 |
| NicDuic Quit Smoking Nicotine Patches | 85835-003 | Patch | Over the counter monograph drugs | August 27, 2025 |
| Quit Smoking Nicotine Patches | 85835-001 | Patch | Over the counter monograph drugs | June 30, 2025 |
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.