NDC 76420-812 – Bupropion Hydrochloride

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

Human Prescription Drug

Product NDC76420-812

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA077285
Marketed since
February 17, 2015
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
76420-812-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-812-01)May 7, 2024
76420-812-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-812-05)May 7, 2024
76420-812-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-812-30)May 7, 2024
76420-812-6060 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-812-60)May 7, 2024
76420-812-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-812-90)May 7, 2024

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