NDC 63187-819 – Bupropion Hydrochloride

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

Human Prescription Drug

Product NDC63187-819

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
Proficient Rx LP
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 (4)

Package NDCDescriptionSince
63187-819-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-819-30)Feb 1, 2017
63187-819-6060 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-819-60)Feb 1, 2017
63187-819-78180 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-819-78)Feb 1, 2017
63187-819-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-819-90)Feb 1, 2017

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