NDC 70518-4264 – Bupropion Hydrochloride

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

Human Prescription Drug

Product NDC70518-4264

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203013
Marketed since
January 24, 2025
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
70518-4264-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-4264-0)Jan 24, 2025

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