NDC 68084-708-25
BuPROPion Hydrochloride 150 mg/1
bupropion hydrochloride · TABLET, FILM COATED, EXTENDED RELEASE
BuPROPion Hydrochloride is a tablet, film coated, extended release containing bupropion hydrochloride at a strength of 150 mg/1. Manufactured by American Health Packaging.
Key Facts
- Brand Name
- BuPROPion Hydrochloride
- Generic Name
- bupropion hydrochloride
- NDC Code (Package)
68084-708-25- NDC Code (Product)
68084-708- Manufacturer
- American Health Packaging
- Strength
- 150 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA079095
- Marketing Start
- 04/01/2015
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.