Bupropion Hydrochloride 68788-8769
Product NDC
68788-8769- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 19, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA216800
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bupropion Hydrochloride | 150 mg/1 |
Drug Class
Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]
Packaging Options(6)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-1)
20 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-2)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-3)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-6)
120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-8)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-9)