NDC 68071-2577 – Bupropion Hydrochloride

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

Human Prescription Drug

Product NDC68071-2577

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076143
Marketed since
January 17, 2006
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
68071-2577-330 TABLET, FILM COATED in 1 BOTTLE (68071-2577-3)Nov 17, 2021
68071-2577-990 TABLET, FILM COATED in 1 BOTTLE (68071-2577-9)Jan 23, 2025

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