NDC 0703-0666
Treprostinil 20 mg per 20 mL injection, solution
On the label: Teva Parenteral Medicines, Inc..
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 Teva Parenteral Medicines, Inc. names for other drugs.
Product details
- Generic drug
- Treprostinil: every company that makes it
- Form
- injection, solution, intravenous; subcutaneous
- Strength
- 20 mg per 20 mL
- Approval
- ANDA ANDA206648
- On the market since
- Sep 30, 2019
- Package NDCs
0703-0666-01- Official label
- DailyMed (National Library of Medicine), updated May 1, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?