NDC 24208-342
Desmopressin Acetate 0.1 mg per 1 mL solution
On the label: Bausch & Lomb Incorporated.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bausch Health Companies Inc. | Laval, Canada | Makes it | No problems foundJan 19, 2024 · 9 inspections |
Product details
- Generic drug
- Desmopressin: every company that makes it
- Form
- solution, nasal
- Strength
- 0.1 mg per 1 mL
- Approval
- ANDA ANDA074830
- On the market since
- Jan 25, 1999
- Package NDCs
24208-342-05- Official label
- DailyMed (National Library of Medicine), updated Sep 1, 2021
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