NDC 63187-176 – Bupropion hydrochloride

Bupropion Hydrochloride 100 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC63187-176

Product details

Brand name
Bupropion hydrochloride
Generic name
Bupropion hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078866
Marketed since
April 8, 2010
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
63187-176-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-176-30)May 1, 2014
63187-176-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-176-60)May 1, 2014
63187-176-78180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-176-78)May 1, 2014

Other Bupropion hydrochloride products