NDC 67046-0699 – Bupropion Hydrochloride XL

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

Human Prescription Drug

Product NDC67046-0699

Product details

Brand name
Bupropion Hydrochloride XL
Generic name
Bupropion Hydrochloride
Labeler
Coupler LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090693
Marketed since
May 6, 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
67046-0699-330 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-0699-3)May 6, 2026

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