NDC 70010-126-03
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 Granules Pharmaceuticals Inc..
Key Facts
- Brand Name
- BUPROPION HYDROCHLORIDE
- Generic Name
- bupropion hydrochloride
- NDC Code (Package)
70010-126-03- NDC Code (Product)
70010-126- Manufacturer
- Granules Pharmaceuticals Inc.
- Strength
- 150 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA218385
- Marketing Start
- 03/31/2025
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.