NDC 69097-876 – Bupropion Hydrochloride (XL)

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

Human Prescription Drug 1 recall

Product NDC69097-876

Product details

Brand name
Bupropion Hydrochloride (XL)
Generic name
Bupropion hydrochloride
Labeler
CIPLA USA INC.,
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA206556
Marketed since
August 29, 2016
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
69097-876-0230 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-876-02)Aug 29, 2016
69097-876-12500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-876-12)Aug 29, 2016

Recalls mentioning this NDC

Other Bupropion hydrochloride products