Nortriptyline Hydrochloride 70771-1614
Product NDC
70771-1614- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 10, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA213441
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Nortriptyline Hydrochloride | 50 mg/1 |
Drug Class
Tricyclic Antidepressant [EPC]
Packaging Options(3)
100 CAPSULE in 1 BOTTLE (70771-1614-1)
30 CAPSULE in 1 BOTTLE (70771-1614-3)
500 CAPSULE in 1 BOTTLE (70771-1614-5)