Bupropion Hydrochloride 72189-0134
Product NDC
72189-0134- Manufacturer
- Direct Rx
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 15, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA210497
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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(4)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-30)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-60)
120 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-72)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-90)