NDC 72516-036 – buPropion Hydrochloride XL

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

Human Prescription Drug

Product NDC72516-036

Product details

Brand name
buPropion Hydrochloride XL
Generic name
Bupropion hydrochloride
Labeler
Oryza pharmaceuticals Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA211200
Marketed since
September 6, 2019
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
72516-036-0330 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-036-03)Sep 6, 2019
72516-036-0990 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-036-09)Sep 6, 2019
72516-036-50500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-036-50)Sep 6, 2019

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