Paroxetine Hydrochloride 69584-0672
Product NDC
69584-0672- Manufacturer
- Oxford Pharmaceuticals, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 14, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA076968
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Paroxetine Hydrochloride | 20 mg/1 |
Drug Class
Serotonin Reuptake Inhibitor [EPC]Serotonin Uptake Inhibitors [MoA]
Packaging Options(5)
30 TABLET, FILM COATED in 1 BOTTLE (69584-672-03)
90 TABLET, FILM COATED in 1 BOTTLE (69584-672-09)
100 TABLET, FILM COATED in 1 BOTTLE (69584-672-10)
500 TABLET, FILM COATED in 1 BOTTLE (69584-672-50)
1000 TABLET, FILM COATED in 1 BOTTLE (69584-672-90)