NDC 31722-833 – Entecavir

Entecavir Anhydrous .5 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC31722-833

Product details

Brand name
Entecavir
Generic name
Entecavir
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205740
Marketed since
August 21, 2015
Listing expires
December 31, 2026
Pharmacologic class
Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Entecavir →

Package NDC codes (4)

Package NDCDescriptionSince
31722-833-3030 TABLET in 1 BOTTLE (31722-833-30)Aug 21, 2015
31722-833-3110 TABLET in 1 BLISTER PACK (31722-833-31)Aug 21, 2015
31722-833-32100 TABLET in 1 CARTON (31722-833-32)Aug 21, 2015
31722-833-9090 TABLET in 1 BOTTLE (31722-833-90)Aug 21, 2015

Recalls mentioning this NDC

Other Entecavir products