NDC 68071-3594 – Bupropion Hydrochloride XL

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

Human Prescription Drug

Product NDC68071-3594

Product details

Brand name
Bupropion Hydrochloride XL
Generic name
Bupropion hydrochloride
Labeler
NuCare Pharmacueticals, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210015
Marketed since
April 30, 2023
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
68071-3594-330 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68071-3594-3)Apr 9, 2024

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