NDC 42806-414 – Bupropion Hydrochloride XL

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

Human Prescription Drug

Product NDC42806-414

Product details

Brand name
Bupropion Hydrochloride XL
Generic name
Bupropion hydrochloride
Labeler
Epic Pharma, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210015
Marketed since
April 30, 2023
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
42806-414-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42806-414-05)Apr 30, 2023
42806-414-0990 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42806-414-09)Apr 30, 2023
42806-414-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42806-414-30)Apr 30, 2023

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