Bupropion hydrochloride (XL) 150 mg/1
Bupropion hydrochloride · TABLET, EXTENDED RELEASE · Lannett Company Inc.
Bupropion hydrochloride (XL) is a tablet, extended release containing bupropion hydrochloride at 150 mg/1, taken oral. Manufactured by Lannett Company Inc..
Key Facts
- Brand Name
- Bupropion hydrochloride (XL)
- Generic Name
- Bupropion hydrochloride
- NDC Code (Product)
0527-2415- Manufacturer
- Lannett Company Inc.
- Strength
- 150 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA208652
- Marketing Start
- 01/08/2018
Recall History
No Recall HistoryFrequently Asked Questions
What is Bupropion hydrochloride (XL) used for?
Bupropion hydrochloride (XL) contains Bupropion hydrochloride. It is a tablet, extended release taken oral. Consult your doctor for specific uses.
Is Bupropion hydrochloride (XL) a controlled substance?
Bupropion hydrochloride (XL) is not classified as a controlled substance by the DEA.
What is the generic name for Bupropion hydrochloride (XL)?
The generic name for Bupropion hydrochloride (XL) is Bupropion hydrochloride. There are 12 other brand versions of Bupropion hydrochloride.
What is the NDC code for Bupropion hydrochloride (XL) 150 mg/1?
The NDC (National Drug Code) for Bupropion hydrochloride (XL) 150 mg/1 is 0527-2415, listed by Lannett Company Inc..
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)