bupropion hydrochloride SR 200 mg/1

bupropion hydrochloride · TABLET, FILM COATED, EXTENDED RELEASE · Solco Healthcare US LLC

No Recall History

Plain English

bupropion hydrochloride SR is a tablet, film coated, extended release containing bupropion hydrochloride at 200 mg/1, taken oral. Manufactured by Solco Healthcare US LLC.

Key Facts

Brand Name: bupropion hydrochloride SR
Generic Name: bupropion hydrochloride
NDC Code (Product): 43547-290
Manufacturer: Solco Healthcare US LLC
Strength: 200 mg/1
Dosage Form: TABLET, FILM COATED, EXTENDED RELEASE
Route: ORAL
Marketing Status
Application #: ANDA202304
Marketing Start: 11/01/2014

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug ineffective1,893 reports

headache1,386 reports

depression1,322 reports

fatigue1,291 reports

nausea1,108 reports

off label use990 reports

pain907 reports

drug interaction854 reports

anxiety846 reports

rash785 reports

Frequently Asked Questions

What is bupropion hydrochloride SR used for?

bupropion hydrochloride SR contains bupropion hydrochloride. It is a tablet, film coated, extended release taken oral. Consult your doctor for specific uses.

Is bupropion hydrochloride SR a controlled substance?

bupropion hydrochloride SR is not classified as a controlled substance by the DEA.

What is the generic name for bupropion hydrochloride SR?

The generic name for bupropion hydrochloride SR is bupropion hydrochloride. There are 12 other brand versions of bupropion hydrochloride.

What is the NDC code for bupropion hydrochloride SR 200 mg/1?

The NDC (National Drug Code) for bupropion hydrochloride SR 200 mg/1 is 43547-290, listed by Solco Healthcare US LLC.

Product NDC

43547-290

Package NDC

43547-290-06

Other Bupropion Brands

See all →

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)