Bupropion Hydrochloride 71335-1214
Product NDC
71335-1214- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 25, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA210497
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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(6)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-1)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-2)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-3)
120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-4)
8 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-5)
180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-6)