NDC 43547-289 – bupropion hydrochloride SR

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

Human Prescription Drug

Product NDC43547-289

Product details

Brand name
bupropion hydrochloride SR
Generic name
bupropion hydrochloride
Labeler
Solco Healthcare US LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA202304
Marketed since
November 1, 2014
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
43547-289-0660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-289-06)Nov 1, 2014
43547-289-0990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-289-09)Nov 1, 2014
43547-289-10100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-289-10)Nov 1, 2014
43547-289-25250 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-289-25)Nov 1, 2014
43547-289-50500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-289-50)Nov 1, 2014

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