50090-2904 : Bupropion Hydrochloride 150 mg Oral Tablet, Film Coated, Extended Release

NDC:	50090-2904
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Bupropion Hydrochloride
Dosage Form:	Oral Tablet, Film Coated, Extended Release
Application #:	ANDA077284
Rev. Date:	Jun 12, 2007

NDC Package Codes:

50090-2904-0: 29 BLISTER PACK IN 1 BOX, UNIT‑DOSE (50090‑2904‑0) > 1 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BLISTER PACK

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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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.