NDCFind

Valacyclovir Hydrochloride 71335-0708-03

Package NDC

71335-0708-03

Product NDC: 71335-0708

Manufacturer
Bryant Ranch Prepack
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
May 24, 2010
Listing Expires
December 31, 2026
Application
ANDA090682
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Active Ingredients

IngredientStrength
Valacyclovir Hydrochloride500 mg/1

Drug Class

DNA Polymerase Inhibitors [MoA]Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]

Selected Package

71335-0708-03Selected

4 TABLET, FILM COATED in 1 BOTTLE (71335-0708-3)

Other packages for this product(9)

60 TABLET, FILM COATED in 1 BOTTLE (71335-0708-0)

15 TABLET, FILM COATED in 1 BOTTLE (71335-0708-1)

10 TABLET, FILM COATED in 1 BOTTLE (71335-0708-2)

7 TABLET, FILM COATED in 1 BOTTLE (71335-0708-4)

20 TABLET, FILM COATED in 1 BOTTLE (71335-0708-5)

30 TABLET, FILM COATED in 1 BOTTLE (71335-0708-6)

8 TABLET, FILM COATED in 1 BOTTLE (71335-0708-7)

90 TABLET, FILM COATED in 1 BOTTLE (71335-0708-8)

14 TABLET, FILM COATED in 1 BOTTLE (71335-0708-9)