Doxepin Hydrochloride 81469-0417
Product NDC
81469-0417- Manufacturer
- First Nation Group, Llc
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 11, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA215710
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Doxepin Hydrochloride | 50 mg/1 |
Drug Class
Tricyclic Antidepressant [EPC]
Packaging Options(2)
100 CAPSULE in 1 BOTTLE (81469-417-01)
500 CAPSULE in 1 BOTTLE (81469-417-05)