NDC 24979-248 – Bupropion hydrochloride

Bupropion Hydrochloride 450 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC24979-248

Product details

Brand name
Bupropion hydrochloride
Generic name
Bupropion hydrochloride
Labeler
Upsher-Smith Laboratories, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA022497
Marketed since
December 15, 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
24979-248-0630 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-248-06)Dec 15, 2023

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