NDC 63187-726 – Bupropion Hydrochloride SR

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

Human Prescription Drug

Product NDC63187-726

Product details

Brand name
Bupropion Hydrochloride SR
Generic name
Bupropion hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA079095
Marketed since
July 2, 2009
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
63187-726-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-726-30)Jul 1, 2016
63187-726-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-726-60)Jul 1, 2016
63187-726-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-726-90)Jul 1, 2016

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