NDC 70518-4446 – Bupropion Hydrochloride XL

Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC70518-4446

Product details

Brand name
Bupropion Hydrochloride XL
Generic name
Bupropion Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090693
Marketed since
August 18, 2025
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
70518-4446-030 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4446-0)Aug 18, 2025

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