NDC 76420-923 – Bupropion Hydrochloride XL

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

Human Prescription Drug

Product NDC76420-923

Product details

Brand name
Bupropion Hydrochloride XL
Generic name
Bupropion Hydrochloride
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA077715
Marketed since
November 26, 2008
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
76420-923-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (76420-923-01)Feb 25, 2025
76420-923-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (76420-923-05)Feb 25, 2025
76420-923-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (76420-923-30)Feb 25, 2025
76420-923-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (76420-923-60)Feb 25, 2025
76420-923-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (76420-923-90)Feb 25, 2025

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