NDC 55154-8180 – Bupropion Hydrochloride

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

Human Prescription Drug

Product NDC55154-8180

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
Cardinal Health 107, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076143
Marketed since
January 29, 2018
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
55154-8180-010 BLISTER PACK in 1 BAG (55154-8180-0) / 1 TABLET, FILM COATED in 1 BLISTER PACKJan 29, 2018

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