NDC 0904-7099 – bupropion hydrochloride SR

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

Human Prescription Drug

Product NDC0904-7099

Product details

Brand name
bupropion hydrochloride SR
Generic name
Bupropion hydrochloride
Labeler
Major Pharmaceuticals
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA202304
Marketed since
January 21, 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
0904-7099-61100 BLISTER PACK in 1 CARTON (0904-7099-61) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKJan 21, 2026

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