Doxepin Hydrochloride 71921-0165
Product NDC
71921-0165- Manufacturer
- Florida Pharmaceutical Products, Llc
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 1, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA213474
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Doxepin Hydrochloride | 75 mg/1 |
Drug Class
Tricyclic Antidepressant [EPC]
Packaging Options(1)
100 CAPSULE in 1 BOTTLE (71921-165-01)