16590-589 : Budeprion XL 150 mg 24 Hr Extended Release Tablet

NDC:	16590-589
Labeler:	Stat Rx USA LLC
Product Type:	Human Prescription Drug
Drug Name:	Budeprion XL
Dosage Form:	Oral Tablet, Film Coated, Extended Release
Application #:	ANDA077284
Rev. Date:	Dec 14, 2006

Appearance:

Markings:	A101
Shapes:	Round
Colors:	White
Size (mm):	7
Segments: ^*	1
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

16590-589-30: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (16590‑589‑30)
16590-589-60: 60 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (16590‑589‑60)
16590-589-90: 90 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (16590‑589‑90)

Active Ingredients:

Bupropion Hydrochloride

Dosage Strength:

150 mg

Inactive Ingredients:

Ethylcellulose
Hydroxypropyl Cellulose
Povidone
Silicon Dioxide
Hydrochloric Acid
Alcohol

Pharmaceutical Classes:

Aminoketone [EPC]
Dopamine Uptake Inhibitors [MoA]
Increased Dopamine Activity [PE]
Increased Norepinephrine Activity [PE]
Norepinephrine Uptake Inhibitors [MoA]

NDC QR Code

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NDC 16590-589 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.