NDC 68071-3669
Imipramine Hydrochloride 50 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Oxford Pharmaceuticals, LLC's NDC 69584-427.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Oxford Pharmaceuticals, LLC | Birmingham, AL, United States | Makes it | Problems found, fixed voluntarilyNov 3, 2023 · 3 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Imipramine: every company that makes it
- Form
- tablet, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA040751
- On the market since
- Aug 1, 2020
- Package NDCs
68071-3669-9- Official label
- DailyMed (National Library of Medicine), updated Aug 26, 2024
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