NDC 42806-411 – Bupropion Hydrochloride

Bupropion Hydrochloride 200 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC42806-411

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
Epic Pharma LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA075932
Marketed since
December 15, 2021
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
42806-411-6060 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-411-60)Dec 15, 2021

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