FDA NDC
Bupropion hydrochloride
This name is from the loaded FDA file.
Source: FDA NDC Directory, live from openFDA. Publisher page
- NDC
- 47335-738
- Proprietary name
- Bupropion hydrochloride
- Nonproprietary name
- Bupropion hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Strength
- 200 mg/1
HCPCS J8700 Billable units per 11-digit NDC: 15.