NDC 81952-112
Heparin Sodium 1000 [USP'U] per 1 mL injection, solution
On the label: Hepalink USA Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Shenzhen Hepalink Pharmaceutical Group Co., Ltd. | Shenzhen, China | Makes the active ingredient | Problems found, fixed voluntarilyJun 13, 2025 · 1 inspection |
| Shenzhen Techdow Pharmaceutical Co., Ltd. | Shenzhen, China | Makes it and tests it | Problems found, fixed voluntarilySep 17, 2019 · 3 inspections |
Recalls
- Oct 1, 2026 · Class II · Shenzhen Techdow Pharmaceutical Co., Ltd.
Lack of Assurance of Sterility
Lots: Lot# CU03232A, Exp 1/31/2028
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Heparin: every company that makes it
- Form
- injection, solution, intravenous; subcutaneous
- Strength
- 1000 [USP'U] per 1 mL
- Approval
- ANDA ANDA202957
- On the market since
- Jun 12, 2014
- Package NDCs
81952-112-0181952-112-0481952-112-0581952-112-0681952-112-0981952-112-10- Official label
- DailyMed (National Library of Medicine), updated Feb 19, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?