NDC 85534-0006 – Bupropion Hydrochloride

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

Human Prescription Drug

Product NDC85534-0006

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
HAWAII REPACK, INC.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA077285
Marketed since
February 17, 2015
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
85534-0006-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-1)Jun 11, 2025
85534-0006-330 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-3)Jun 11, 2025
85534-0006-5500 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-5)Jun 11, 2025
85534-0006-660 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-6)Jun 11, 2025
85534-0006-990 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-9)Jun 11, 2025

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