Home NDC 82868-106
Valacyclovir Hydrochloride
Product NDC 82868-106
11-digit product format 828680106
Labeler code 82868
Product ID 82868-106_5036e4bf-9610-4be3-e063-6294a90abd8c
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name valacyclovir
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Northwind Health Company, LLC
Application ANDA078518
Marketing category ANDA
Marketing start 2026-04-21
Substance VALACYCLOVIR HYDROCHLORIDE
Active strength 1 g/1
Pharmacologic classes DNA Polymerase Inhibitors [MoA], Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [EXT]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Valacyclovir Hydrochloride
Listing expiration 2027-12-31
Active Ingredients# Ingredient, Strength table Ingredient Strength VALACYCLOVIR HYDROCHLORIDE 1 g/1
Harmonized Identifiers# Field, Values table Field Values Unii G447S0T1VC Rxcui 313564
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 82868-106-21 Valacyclovir Hydrochloride 21 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 21 1
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 82868-106-21 82868010621 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-106-21) 2026-04-21 No No Historical