NDC 82804-127 – Bupropion Hydrochloride

Bupropion Hydrochloride 75 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC82804-127

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076143
Marketed since
January 17, 2006
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
82804-127-3030 TABLET, FILM COATED in 1 BOTTLE (82804-127-30)Jul 18, 2024

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