NDC 0904-7505 – Bupropion Hydrochloride XL

Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC0904-7505

Product details

Brand name
Bupropion Hydrochloride XL
Generic name
Bupropion Hydrochloride
Labeler
Major Pharmaceuticals
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090693
Marketed since
November 25, 2024
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

Uses, dosage, side effects and warnings for Bupropion hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
0904-7505-0430 BLISTER PACK in 1 CARTON (0904-7505-04) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACKNov 25, 2024
0904-7505-61100 BLISTER PACK in 1 CARTON (0904-7505-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACKNov 25, 2024

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