BuPROPion Hydrochloride 150 mg/1
bupropion hydrochloride · TABLET, FILM COATED, EXTENDED RELEASE · American Health Packaging
BuPROPion Hydrochloride is a tablet, film coated, extended release containing bupropion hydrochloride at 150 mg/1, taken oral. Manufactured by American Health Packaging.
Key Facts
- Brand Name
- BuPROPion Hydrochloride
- Generic Name
- bupropion hydrochloride
- NDC Code (Product)
68084-708- Manufacturer
- American Health Packaging
- Strength
- 150 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA079095
- Marketing Start
- 04/01/2015
Recall History
No Recall HistoryFrequently Asked Questions
What is BuPROPion Hydrochloride used for?
BuPROPion Hydrochloride contains bupropion hydrochloride. It is a tablet, film coated, extended release taken oral. Consult your doctor for specific uses.
Is BuPROPion Hydrochloride a controlled substance?
BuPROPion Hydrochloride is not classified as a controlled substance by the DEA.
What is the generic name for BuPROPion Hydrochloride?
The generic name for BuPROPion Hydrochloride is bupropion hydrochloride. There are 12 other brand versions of bupropion hydrochloride.
What is the NDC code for BuPROPion Hydrochloride 150 mg/1?
The NDC (National Drug Code) for BuPROPion Hydrochloride 150 mg/1 is 68084-708, listed by American Health Packaging.
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)