Bupropion Hydrochloride 71335-2457
Product NDC
71335-2457- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 31, 2023
- 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(9)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-1)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-2)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-3)
120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-4)
45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-5)
180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-6)
28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-7)
56 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-8)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-9)