Home NDC 48433-144
Valacyclovir Hydrochloride
Product NDC 48433-144
11-digit product format 484330144
Labeler code 48433
Product ID 48433-144_4ee1037d-94f5-562f-e063-6394a90af03d
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name valacyclovir
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Safecor Health LLC
Application ANDA078518
Marketing category ANDA
Marketing start 2026-04-03
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 Hydrochloride
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 48433-144-01 Valacyclovir Hydrochloride 1 in 1 BLISTER PACK TABLET, FILM COATED 1 2 48433-144-03 Valacyclovir Hydrochloride 30 in 1 CARTON TABLET, FILM COATED 30 2
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 48433-144-01 48433014401 1 in 1 BLISTER PACK Historical 48433-144-03 48433014403 30 BLISTER PACK in 1 CARTON (48433-144-03) / 1 TABLET, FILM COATED in 1 BLISTER PACK (48433-144-01) 30 blister pack 2026-04-03 No No Current