Registered establishment in Tianchang, Anhui, China. 1 device type, 1 clearance.
Anhui Tianyang Pharmaceutical Co., Ltd. is a manufacturer holding a current FDA establishment registration. The registration covers Saline, Vascular Access Flush. Its earliest product listing with the FDA dates from 2023.
Registration
FDA registration record for Anhui Tianyang Pharmaceutical Co., Ltd. | Registered name | ANHUI TIANYANG PHARMACEUTICAL CO., LTD |
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3016972038 |
| FEI number | 3016972038 |
| Establishment type | Manufacturer |
Chinese Registration
Chinese company register details for Anhui Tianyang Pharmaceutical Co., Ltd. | Chinese legal name | 安徽天洋药业有限公司 |
| Unified social credit code | 913411007690034033 |
| Source | NMPA UDI database |
Location
Address of Anhui Tianyang Pharmaceutical Co., Ltd. | City | Tianchang |
| Province | Anhui |
| Address | NO.46 Tiantong Road |
| Postal code | 239304 |
| Country | China |
From the Company
Published by the company on its own website, not by the FDA.
Information published by Anhui Tianyang Pharmaceutical Co., Ltd. | Founded | 1994 |
| Factory area | 125亩 |
| Main products | Chinese medicine extraction dosage forms, Large-volume injections, Suppositories, Solution dosage forms |
| Certifications | GMP, National high-tech enterprise, AAA credit rating |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.