NDC 43602-269
hydromorphone hydrochloride 32 mg tablet, extended release
On the label: Ascent Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ascent Pharmaceuticals Inc | Central Islip, NY, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections |
Product details
- Generic drug
- Hydromorphone: every company that makes it
- Form
- tablet, extended release
- Strength
- 32 mg
- Approval
- ANDA ANDA212133
- On the market since
- Sep 24, 2020
- Package NDCs
43602-269-0543602-269-30- Official label
- DailyMed (National Library of Medicine), updated Sep 24, 2020
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