NDC 42806-413 – Bupropion Hydrochloride SR

Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC42806-413

Product details

Brand name
Bupropion Hydrochloride SR
Generic name
Bupropion hydrochloride
Labeler
Epic Pharma, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA216766
Marketed since
February 28, 2023
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
42806-413-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-413-60)Feb 28, 2023

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