Bupropion Hydrochloride 31722-0067
Product NDC
31722-0067- Manufacturer
- Camber Pharmaceuticals, Inc.
- 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(5)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-067-01)
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-067-05)
250 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-067-25)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-067-60)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-067-90)