NDC 60505-0158 – Bupropion Hydrochloride

Bupropion Hydrochloride 75 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC60505-0158

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
Apotex Corp
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076143
Marketed since
January 17, 2006
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
60505-0158-1100 TABLET, FILM COATED in 1 BOTTLE (60505-0158-1)Jan 17, 2006
60505-0158-330 TABLET, FILM COATED in 1 BOTTLE (60505-0158-3)Jan 17, 2006
60505-0158-5500 TABLET, FILM COATED in 1 BOTTLE (60505-0158-5)Jan 17, 2006
60505-0158-71000 TABLET, FILM COATED in 1 BOTTLE (60505-0158-7)Jan 17, 2006
60505-0158-990 TABLET, FILM COATED in 1 BOTTLE (60505-0158-9)Jan 17, 2006

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