NDC 51267-890 – Contrave Extended-Release

Naltrexone Hydrochloride 8 mg/1; Bupropion Hydrochloride 90 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug 2 recalls

Product NDC51267-890

Product details

Brand name
Contrave Extended-Release
Generic name
Naltrexone hydrochloride and bupropion hydrochloride
Labeler
Nalpropion Pharmaceuticals LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
NDA · NDA200063
Marketed since
October 22, 2014
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone; Opioid Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Contrave →

Package NDC codes (2)

Package NDCDescriptionSince
51267-890-07 sample7 TABLET, EXTENDED RELEASE in 1 BOTTLE (51267-890-07)Jan 14, 2021
51267-890-99120 TABLET, EXTENDED RELEASE in 1 BOTTLE (51267-890-99)Oct 22, 2014

Recalls mentioning this NDC