Bupropion Hydrochloride 68788-8815
Product NDC
68788-8815- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 21, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA215568
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bupropion Hydrochloride | 300 mg/1 |
Drug Class
Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]
Packaging Options(5)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8815-1)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8815-3)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8815-6)
120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8815-8)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8815-9)