Imipramine Hydrochloride 72789-0492
Product NDC
72789-0492- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 7, 2016
- Listing Expires
- December 31, 2027
- 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, PLASTIC (72789-492-01)
1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-492-95)