NDC 68382-920 – Entecavir

Entecavir .5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 4 recalls

Product NDC68382-920

Product details

Brand name
Entecavir
Generic name
Entecavir
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206745
Marketed since
August 10, 2017
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
68382-920-01100 TABLET, FILM COATED in 1 BOTTLE (68382-920-01)Aug 10, 2017
68382-920-0630 TABLET, FILM COATED in 1 BOTTLE (68382-920-06)Aug 10, 2017
68382-920-1690 TABLET, FILM COATED in 1 BOTTLE (68382-920-16)Aug 10, 2017
68382-920-7710 BLISTER PACK in 1 CARTON (68382-920-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-920-30)Aug 10, 2017

Recalls mentioning this NDC

Other Entecavir products