Home NDC 67046-1347 Valacyclovir
Product NDC 67046-1347
11-digit product format 670461347
Labeler code 67046
Product ID 67046-1347_5100e0ed-43ff-f8a5-e063-6294a90a8d75
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Valacyclovir
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Coupler LLC
Application ANDA203047
Marketing category ANDA
Marketing start 2026-05-04
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
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 67046-1347-3 Valacyclovir 30 in 1 BLISTER PACK TABLET, FILM COATED 30 1
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 67046-1347-3 67046134703 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1347-3) 2026-05-04 No No Current