NDC 87441-014 – Bupropion hydrochloride

Bupropion Hydrochloride 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC87441-014

Product details

Brand name
Bupropion hydrochloride
Generic name
Bupropion hydrochloride
Labeler
Unit Dose Solutions, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA215568
Marketed since
June 8, 2026
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
87441-014-0130 TABLET in 1 BLISTER PACK (87441-014-01)Jun 8, 2026

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