NDC 69097-072-12
Bupropion Hydrochloride 300 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 300 mg/1. Manufactured by Cipla USA., Inc..
Key Facts
- Brand Name
- Bupropion Hydrochloride
- Generic Name
- Bupropion hydrochloride
- NDC Code (Package)
69097-072-12- NDC Code (Product)
69097-072- Manufacturer
- Cipla USA., Inc.
- Strength
- 300 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA207479
- Marketing Start
- 10/25/2023
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.