Home NDC 68071-3624
Valacyclovir
Product NDC 68071-3624
11-digit product format 680713624
Labeler code 68071
Product ID 68071-3624_1ac7a6de-4617-c142-e063-6394a90a4d71
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Valacyclovir
Dosage form TABLET
Route ORAL
Labeler NuCare Pharmaceuticals,Inc.
Application ANDA209553
Marketing category ANDA
Marketing start 2023-02-14
Substance VALACYCLOVIR HYDROCHLORIDE
Active strength 1000 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 1000 mg/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 68071-3624-3 Valacyclovir 30 in 1 BOTTLE TABLET 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68071-3624 VALACYCLOVIR TABLET [NUCARE PHARMACEUTICALS,INC.] 1 Current NDC, 1 package rows 20240615_1ac7a13e-3f30-e140-e063-6394a90aa09d.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 68071-3624-3 68071362403 30 TABLET in 1 BOTTLE (68071-3624-3) 30 tablet 2024-06-13 No No Current