NDC 70518-4081 – Bupropion hydrochloride

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

Human Prescription Drug

Product NDC70518-4081

Product details

Brand name
Bupropion hydrochloride
Generic name
Bupropion hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA216800
Marketed since
May 16, 2024
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
70518-4081-130 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4081-1)Sep 26, 2024
70518-4081-260 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4081-2)Jul 1, 2025
70518-4081-390 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4081-3)Jul 1, 2025
70518-4081-430 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4081-4)Aug 27, 2025

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