Imipramine Hydrochloride 69315-0134
Product NDC
69315-0134- Manufacturer
- Leading Pharma, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 7, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA040903
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Imipramine Hydrochloride | 25 mg/1 |
Drug Class
Tricyclic Antidepressant [EPC]
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE (69315-134-01)
1000 TABLET, FILM COATED in 1 BOTTLE (69315-134-10)