NDC 50090-4749 – Bupropion Hydrochloride

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

Human Prescription Drug

Product NDC50090-4749

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
A-S Medication Solutions
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090693
Marketed since
June 14, 2017
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
50090-4749-030 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4749-0)Nov 22, 2019
50090-4749-190 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4749-1)Nov 22, 2019

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