NDC 77771-144 – Bupropion Hydrochloride (XL)

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

Human Prescription Drug

Product NDC77771-144

Product details

Brand name
Bupropion Hydrochloride (XL)
Generic name
Bupropion hydrochloride
Labeler
RADHA PHARMACEUTICALS, INC.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA207479
Marketed since
October 26, 2022
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
77771-144-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-144-05)Oct 26, 2022
77771-144-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-144-30)Oct 26, 2022
77771-144-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-144-90)Oct 26, 2022

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