NDC 23155-578 – Desipramine Hydrochloride
Desipramine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC23155-578
Product details
- Brand name
- Desipramine Hydrochloride
- Generic name
- Desipramine hydrochloride
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207433
- Marketed since
- November 1, 2016
- Marketing end
- September 30, 2026
- Pharmacologic class
- Tricyclic Antidepressant
Active ingredients
- Desipramine Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Desipramine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 23155-578-01 | 100 TABLET in 1 BOTTLE (23155-578-01) | Nov 1, 2016 |
Recalls mentioning this NDC
- D-0107-2026 Nov 5, 2025 · Class II
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level. - D-0108-2026 Nov 5, 2025 · Class II
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level. - D-0111-2026 Nov 5, 2025 · Class II
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level. - D-0112-2026 Nov 5, 2025 · Class II
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level. - D-0109-2026 Nov 5, 2025 · Class II
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level. - D-0110-2026 Nov 5, 2025 · Class II
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
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