Bupropion Hydrochloride 00615-8581
Product NDC
00615-8581- Manufacturer
- Ncs Healthcare Of Ky, Llc Dba Vangard Labs
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 25, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA075491
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bupropion Hydrochloride | 75 mg/1 |
Drug Class
Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]
Packaging Options(1)
30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8581-39)