NDC 16729-444 – Bupropion Hydrochloride

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

Human Prescription Drug

Product NDC16729-444

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
Accord Healthcare Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210497
Marketed since
March 25, 2019
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
16729-444-1030 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-444-10)Mar 25, 2019
16729-444-16500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-444-16)Mar 25, 2019

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