NDC 80425-0300 – Bupropion hydrochloride

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

Human Prescription Drug

Product NDC80425-0300

Product details

Brand name
Bupropion hydrochloride
Generic name
Bupropion hydrochloride
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210497
Marketed since
April 6, 2023
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
80425-0300-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0300-1)Apr 6, 2023
80425-0300-260 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0300-2)Apr 6, 2023
80425-0300-390 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0300-3)Apr 6, 2023

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