Home NDC 72189-630 Valacyclovir
Product NDC 72189-630
11-digit product format 721890630
Labeler code 72189
Product ID 72189-630_3c6c3546-b4a4-1f0e-e063-6394a90a8c29
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Valacyclovir
Dosage form TABLET
Route ORAL
Labeler Direct_Rx
Application ANDA209553
Marketing category ANDA
Marketing start 2025-06-26
Substance VALACYCLOVIR HYDROCHLORIDE
Active strength 500 mg/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 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Valacyclovir
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength VALACYCLOVIR HYDROCHLORIDE 500 mg/1
Harmonized Identifiers# Field, Values table Field Values Unii G447S0T1VC Rxcui 313565
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72189-630-20 Valacyclovir 20 in 1 BOTTLE TABLET 20 3 72189-630-30 Valacyclovir 20 in 1 BOTTLE TABLET 20 3
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 72189-630-20 72189063020 20 TABLET in 1 BOTTLE (72189-630-20) 20 tablet 2025-06-26 No No Current 72189-630-30 72189063030 20 TABLET in 1 BOTTLE (72189-630-30) 20 tablet 2025-06-26 No No Current