NDC 50228-176 – Bupropion Hydrochloride SR

Bupropion Hydrochloride 200 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC50228-176

Product details

Brand name
Bupropion Hydrochloride SR
Generic name
Bupropion hydrochloride
Labeler
ScieGen Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA205794
Marketed since
April 20, 2018
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
50228-176-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-176-01)Apr 20, 2018
50228-176-101000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-176-10)Apr 20, 2018
50228-176-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-176-30)Apr 20, 2018
50228-176-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-176-60)Apr 20, 2018

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