NDC 69680-158 – Bupropion hydrochloride (XL)

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

Human Prescription Drug

Product NDC69680-158

Product details

Brand name
Bupropion hydrochloride (XL)
Generic name
Bupropion hydrochloride
Labeler
Vitruvias Therapeutics
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA208652
Marketed since
April 10, 2023
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

Uses, dosage, side effects and warnings for Bupropion Hydrochloride (XL) →

Package NDC codes (4)

Package NDCDescriptionSince
69680-158-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-158-30)Apr 10, 2023
69680-158-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-158-90)Apr 10, 2023
69680-158-92500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-158-92)Apr 10, 2023
69680-158-931000 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-158-93)Apr 10, 2023

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