NDC 67046-1587 – Bupropion Hydrochloride

Bupropion Hydrochloride 75 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC67046-1587

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
Coupler LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206975
Marketed since
September 16, 2025
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
67046-1587-330 TABLET in 1 BLISTER PACK (67046-1587-3)Sep 16, 2025

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