NDC 0115-5445 – Bupropion Hydrochloride

Bupropion Hydrochloride 200 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC0115-5445

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA076711
Marketed since
December 3, 2004
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
0115-5445-1360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-5445-13)Dec 3, 2004

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