NDC 70010-784-09
Bupropion hydrochloride 150 mg/1
Bupropion hydrochloride · TABLET, EXTENDED RELEASE
Bupropion hydrochloride is a tablet, extended release containing bupropion hydrochloride at a strength of 150 mg/1. Manufactured by Granules Pharmaceuticals Inc..
Key Facts
- Brand Name
- Bupropion hydrochloride
- Generic Name
- Bupropion hydrochloride
- NDC Code (Package)
70010-784-09- NDC Code (Product)
70010-784- Manufacturer
- Granules Pharmaceuticals Inc.
- Strength
- 150 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA215568
- Marketing Start
- 12/15/2022
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.