NDC 70518-4591 – bupropion hydrochloride SR

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

Human Prescription Drug

Product NDC70518-4591

Product details

Brand name
bupropion hydrochloride SR
Generic name
Bupropion hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA202304
Marketed since
March 20, 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
70518-4591-030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4591-0)Mar 20, 2026

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