NDC 16729-549
BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE 2 mg / 0.5 mg tablet
On the label: Accord Healthcare Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Wes Pharma Inc | Westminster, MD, United States | Makes it | Problems found, fixed voluntarilyNov 20, 2025 · 7 inspections |
Product details
- Generic drug
- Buprenorphine and Naloxone: every company that makes it
- Form
- tablet, sublingual
- Strength
- 2 mg / 0.5 mg
- Approval
- ANDA ANDA209069
- On the market since
- Sep 1, 2020
- Package NDCs
16729-549-10- Official label
- DailyMed (National Library of Medicine), updated May 3, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?