Drugplain

Bupropion Hydrochloride (SR) 150 mg/1

bupropion hydrochloride · TABLET, FILM COATED, EXTENDED RELEASE · ScieGen Pharmaceuticals, Inc.

No Recall History
Plain English

Bupropion Hydrochloride (SR) is a tablet, film coated, extended release containing bupropion hydrochloride at 150 mg/1, taken oral. Manufactured by ScieGen Pharmaceuticals, Inc..

Key Facts

Brand Name
Bupropion Hydrochloride (SR)
Generic Name
bupropion hydrochloride
NDC Code (Product)
50228-338
Manufacturer
ScieGen Pharmaceuticals, Inc.
Strength
150 mg/1
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Marketing Status
Application #
ANDA206122
Marketing Start
05/01/2019

Recall History

No Recall History

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) 150 mg/1?

The NDC (National Drug Code) for Bupropion Hydrochloride (SR) 150 mg/1 is 50228-338, listed by ScieGen Pharmaceuticals, Inc..