NDC 68382-049 – acyclovir

Acyclovir Sodium 50 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug 2 recalls

Product NDC68382-049

Product details

Brand name
acyclovir
Generic name
Acyclovir
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA206535
Marketed since
November 27, 2018
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 (1)

Package NDCDescriptionSince
68382-049-1010 VIAL, SINGLE-USE in 1 CARTON (68382-049-10) / 20 mL in 1 VIAL, SINGLE-USE (68382-049-01)Nov 27, 2018

Recalls mentioning this NDC

Other Acyclovir products