Home NDC 70518-4661
Valacyclovir
Product NDC 70518-4661
11-digit product format 705184661
Labeler code 70518
Product ID 70518-4661_52184b4f-f400-eeb8-e063-6294a90ab18f
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Valacyclovir
Dosage form TABLET
Route ORAL
Labeler REMEDYREPACK INC.
Application ANDA209553
Marketing category ANDA
Marketing start 2026-05-14
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 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Valacyclovir
Listing expiration 2027-12-31
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 70518-4661-0 Valacyclovir 30 in 1 BOTTLE, PLASTIC TABLET 30 1
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 70518-4661-0 70518466100 30 TABLET in 1 BOTTLE, PLASTIC (70518-4661-0) 30 tablet 2026-05-14 No No Historical