NDC 23155-489
Desmopressin Acetate 0.1 mg tablet
On the label: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc. | East Brunswick, NJ, United States | Makes it, tests it, packages it and labels it | No problems foundSep 19, 2023 · 10 inspections |
Recalls
- Nov 23, 2022 · Class II · Heritage Pharmaceuticals Inc
Subpotent Drug
Lots: Lot #: 220440A, Exp. Date 05/2024
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Desmopressin: every company that makes it
- Form
- tablet, oral
- Strength
- 0.1 mg
- Approval
- ANDA ANDA207880
- On the market since
- May 26, 2017
- Package NDCs
23155-489-0123155-489-05- Official label
- DailyMed (National Library of Medicine), updated Mar 30, 2022
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