NDC 70518-3787 – Bupropion Hydrochloride SR

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

Human Prescription Drug

Product NDC70518-3787

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 · ANDA205794
Marketed since
July 12, 2023
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
70518-3787-130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3787-1)Aug 14, 2025

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