50090-7112 : Bupropion Hydrochloride XL 150 mg Oral Tablet, Extended Release

NDC:	50090-7112
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Bupropion Hydrochloride XL
Dosage Form:	Oral Tablet, Extended Release
Application #:	ANDA210015
Rev. Date:	Apr 30, 2023

NDC Package Codes:

50090-7112-0: 90 TABLET, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (50090‑7112‑0)

Active Ingredients:

Bupropion Hydrochloride

Dosage Strength:

150 mg

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 50090-7112 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.