NDC 51655-390 – bupropion Hydrochloride

Bupropion Hydrochloride 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-390

Product details

Brand name
bupropion Hydrochloride
Generic name
bupropion Hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206975
Marketed since
January 28, 2022
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

Uses, dosage, side effects and warnings for Bupropion hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
51655-390-2560 TABLET in 1 BOTTLE, PLASTIC (51655-390-25)Jan 28, 2022
51655-390-2690 TABLET in 1 BOTTLE, PLASTIC (51655-390-26)Jan 28, 2022

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