NDC 70010-126 – Bupropion Hydrochloride

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

Human Prescription Drug

Product NDC70010-126

Product details

Brand name
Bupropion Hydrochloride
Generic name
bupropion hydrochloride
Labeler
Granules Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA218385
Marketed since
March 31, 2025
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
70010-126-0330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-126-03)Mar 31, 2025
70010-126-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-126-05)Mar 31, 2025
70010-126-0660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-126-06)Mar 31, 2025

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