NDC 71205-504 – Bupropion Hydrochloride

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

Human Prescription Drug

Product NDC71205-504

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210497
Marketed since
November 8, 2018
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
71205-504-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-30)Nov 13, 2020
71205-504-6060 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-60)Nov 13, 2020
71205-504-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-90)Nov 13, 2020

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