50090-1768 : Bupropion Hydrochloride 100 mg Oral Tablet, Extended Release

NDC:	50090-1768
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Bupropion Hydrochloride
Dosage Form:	Oral Tablet, Extended Release
Application #:	ANDA075932
Rev. Date:	Nov 25, 2003

Appearance:

Markings:	E;over;410
Shapes:	Round
Colors:	Blue
Size (mm):	8
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.

E over 410: (0185-0410) Bupropion Hydrochloride 100 mg Oral Tablet, Extended Release by A-s Medication Solutions

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:

50090-1768-0: 60 TABLET, EXTENDED RELEASE IN 1 BOTTLE (50090‑1768‑0)
50090-1768-2: 90 TABLET, EXTENDED RELEASE IN 1 BOTTLE (50090‑1768‑2)

Active Ingredients:

Bupropion Hydrochloride

Dosage Strength:

100 mg

Inactive Ingredients:

Carnauba Wax
Fd&c Blue No. 1
Hydroxypropyl Cellulose (Type H)
Magnesium Stearate
Cellulose, Microcrystalline
Polyethylene Glycols
Polysorbate 80
Titanium Dioxide
Hypromelloses

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 50090-1768 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.