NDC 67046-1143 – Bupropion Hydrochloride

Bupropion Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC67046-1143

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
Coupler LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076143
Marketed since
August 3, 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
67046-1143-330 TABLET, FILM COATED in 1 BLISTER PACK (67046-1143-3)Aug 3, 2026

Other bupropion hydrochloride products