50090-4169 : Bupropion Hydrochloride (Xl) (Xl) 150 mg Oral Tablet, Extended Release

NDC:	50090-4169
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Bupropion Hydrochloride (Xl)
Dosage Form:	Oral Tablet, Extended Release
Application #:	ANDA208652
Rev. Date:	Jan 8, 2018

Appearance:

Markings:	ST;150
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:

50090-4169-0: 90 TABLET, EXTENDED RELEASE IN 1 BOTTLE (50090‑4169‑0)
50090-4169-1: 30 TABLET, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (50090‑4169‑1)
50090-4169-2: 60 TABLET, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (50090‑4169‑2)

Active Ingredients:

Bupropion Hydrochloride

Dosage Strength:

150 mg

Inactive Ingredients:

Povidone, Unspecified
Tartaric Acid
Glyceryl Distearate
Magnesium Stearate
Hydroxypropyl Cellulose, Unspecified
Ethylcellulose, Unspecified
Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
Silicon Dioxide
Shellac
Isopropyl Alcohol
Ferrosoferric Oxide
Butyl Alcohol
Propylene Glycol
Ammonia /

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 50090-4169 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.