0093-5351 : 24 Hr Budeprion 300 mg Extended Release Tablet

NDC:	0093-5351
Labeler:	Teva Pharmaceuticals USA Inc
Product Type:	Human Prescription Drug
Drug Name:	Budeprion XL
Dosage Form:	Oral Tablet, Extended Release
Application #:	ANDA077415
Rev. Date:	Dec 15, 2006

Appearance:

Markings:	682
Shapes:	Oval
Colors:	Yellow
Size (mm):	17
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.

682: (0093-5351) 24 Hr Budeprion 300 mg Extended Release Tablet by Teva Pharmaceuticals USA Inc

The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

0093-5351-56: 30 TABLET, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (0093‑5351‑56)

Active Ingredients:

Bupropion Hydrochloride

Dosage Strength:

300 mg

Inactive Ingredients:

Silicon Dioxide
Hydroxypropyl Cellulose (Type H)
Lactose Monohydrate
Magnesium Stearate
Cellulose, Microcrystalline
Fd&c Red No. 40
Fd&c Yellow No. 5
Hypromelloses
Polyethylene Glycols
Polydextrose
Titanium Dioxide
Triacetin

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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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.