WELLBUTRIN XL 150 mg/1
bupropion hydrochloride · TABLET, EXTENDED RELEASE · Bausch Health US LLC
WELLBUTRIN XL is a tablet, extended release containing bupropion hydrochloride at 150 mg/1, taken oral. Manufactured by Bausch Health US LLC.
Key Facts
- Brand Name
- WELLBUTRIN XL
- Generic Name
- bupropion hydrochloride
- NDC Code (Product)
0187-0730- Manufacturer
- Bausch Health US LLC
- Strength
- 150 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- NDA021515
- Marketing Start
- 08/29/2003
Recall History
No Recall HistoryFrequently Asked Questions
What is WELLBUTRIN XL used for?
WELLBUTRIN XL contains bupropion hydrochloride. It is a tablet, extended release taken oral. Consult your doctor for specific uses.
Is WELLBUTRIN XL a controlled substance?
WELLBUTRIN XL is not classified as a controlled substance by the DEA.
What is the generic name for WELLBUTRIN XL?
The generic name for WELLBUTRIN XL is bupropion hydrochloride. There are 12 other brand versions of bupropion hydrochloride.
What is the NDC code for WELLBUTRIN XL 150 mg/1?
The NDC (National Drug Code) for WELLBUTRIN XL 150 mg/1 is 0187-0730, listed by Bausch Health US LLC.
Other Bupropion Brands
See all →- Bupropion Hydrochloride SR150 mg/172162-1529
- Bupropion Hydrochloride300 mg/176420-812
- Bupropion Hydrochloride (XL)300 mg/177771-145
- BUPROPION HYDROCHLORIDE150 mg/180425-0461
- Bupropion Hydrochloride (XL)150 mg/183008-082
- Bupropion Hydrochloride (XL)300 mg/183301-0025
- Bupropion Hydrochloride XL300 mg/10904-7469
- Bupropion Hydrochloride75 mg/10904-7529
- bupropion hydrochloride150 mg/116571-862
- Bupropion Hydrochloride75 mg/124689-119
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)