NDC 0378-4276 – Valacyclovir Hydrochloride

Valacyclovir Hydrochloride 1 g/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC0378-4276

Product details

Brand name
Valacyclovir Hydrochloride
Generic name
valacyclovir
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078518
Marketed since
May 24, 2010
Listing expires
December 31, 2027
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 Valacyclovir Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
0378-4276-7790 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-4276-77)May 24, 2010
0378-4276-9330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-4276-93)May 24, 2010

Recalls mentioning this NDC

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