NDC 70010-785 – Bupropion hydrochloride

Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC70010-785

Product details

Brand name
Bupropion hydrochloride
Generic name
Bupropion hydrochloride
Labeler
Granules Pharmaceuticals Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA215568
Marketed since
December 15, 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
70010-785-0330 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-785-03)Dec 15, 2022
70010-785-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-785-05)Dec 15, 2022
70010-785-0990 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-785-09)Dec 15, 2022

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