NDC 68382-791 – Acyclovir

Acyclovir 400 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC68382-791

Product details

Brand name
Acyclovir
Generic name
Acyclovir
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204314
Marketed since
September 10, 2014
Listing expires
December 31, 2026
Pharmacologic class
Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Acyclovir →

Package NDC codes (6)

Package NDCDescriptionSince
68382-791-01100 TABLET in 1 BOTTLE (68382-791-01)Sep 10, 2014
68382-791-05500 TABLET in 1 BOTTLE (68382-791-05)Sep 10, 2014
68382-791-0630 TABLET in 1 BOTTLE (68382-791-06)Sep 10, 2014
68382-791-101000 TABLET in 1 BOTTLE (68382-791-10)Sep 10, 2014
68382-791-1690 TABLET in 1 BOTTLE (68382-791-16)Sep 10, 2014
68382-791-3010 BLISTER PACK in 1 CARTON (68382-791-30) / 10 TABLET in 1 BLISTER PACKSep 10, 2014

Recalls mentioning this NDC

Other Acyclovir products