Imipramine Hydrochloride 70868-0810
Product NDC
70868-0810- Manufacturer
- Key Therapeutics
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 18, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA040751
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Imipramine Hydrochloride | 25 mg/1 |
Drug Class
Tricyclic Antidepressant [EPC]
Packaging Options(1)
100 TABLET, FILM COATED in 1 BOTTLE (70868-810-10)