Desipramine Hydrochloride 50742-0117
Product NDC
50742-0117- Manufacturer
- Ingenus Pharmaceuticals, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 19, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA204963
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Desipramine Hydrochloride | 150 mg/1 |
Drug Class
Tricyclic Antidepressant [EPC]
Packaging Options(1)
50 TABLET in 1 BOTTLE (50742-117-50)