Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Par Health USA, LLC names for other drugs.
Recalls
- Oct 13, 2026 · Class I · Par Health USA, LLC
Particulate matter: particulate matter identified as cellulose, polystyrene, polyethylene teraphalate, stainless steel, or stopper material in the product solution.
Lots: Lot #: 83449, Exp Date: 10/2026; 82682, Exp Date: 11/2026; 86714, 87302, 87560, Exp Date: 02/2027; 87753, 88401, Exp Date: 03/2027; 88614, 88836, Exp Date: 04/2027; 90220, Exp Date: 05/2027; 91216, 91219, Exp Date: 06/2027; 92004, 92006, Exp Date: 07/2027; 92009, 92596, 92782, 93107, 93329, Exp Dat… - Oct 13, 2026 · Class I · Par Health USA, LLC
Particulate matter: particulate matter identified as cellulose, polystyrene, polyethylene teraphalate, stainless steel, or stopper material in the product solution.
Lots: Lot #: 84193, Exp Date: 10/2026; 92880, Exp Date: 08/2027.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Argatroban: every company that makes it
- Form
- injection, intravenous
- Strength
- 250 mg per 2.5 mL
- Approval
- ANDA ANDA091665
- On the market since
- Jun 1, 2015
- Package NDCs
42023-182-89- Official label
- DailyMed (National Library of Medicine), updated Aug 20, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?