NDC 0615-8581-39
BUPROPION HYDROCHLORIDE 75 mg/1
BUPROPION HYDROCHLORIDE · TABLET, FILM COATED
BUPROPION HYDROCHLORIDE is a tablet, film coated containing bupropion hydrochloride at a strength of 75 mg/1. Manufactured by NCS HealthCare of KY, LLC dba Vangard Labs.
Key Facts
- Brand Name
- BUPROPION HYDROCHLORIDE
- Generic Name
- BUPROPION HYDROCHLORIDE
- NDC Code (Package)
0615-8581-39- NDC Code (Product)
0615-8581- Manufacturer
- NCS HealthCare of KY, LLC dba Vangard Labs
- Strength
- 75 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA075491
- Marketing Start
- 04/25/2024
Recall History
No Recall HistoryView Full Drug Page
BUPROPION HYDROCHLORIDE — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.