Home NDC 60760-757
Valacyclovir Hydrochloride
Product NDC 60760-757
11-digit product format 607600757
Labeler code 60760
Product ID 60760-757_275c0198-10a6-139e-e063-6394a90a72be
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Valacyclovir Hydrochloride
Dosage form TABLET, FILM COATED
Route ORAL
Labeler ST. MARY'S MEDICAL PARK PHARMACY
Application ANDA090682
Marketing category ANDA
Marketing start 2010-05-24
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 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Valacyclovir Hydrochloride
Listing expiration 2026-12-31
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 60760-757-42 Valacyclovir Hydrochloride 42 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 42 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 60760-757 VALACYCLOVIR HYDROCHLORIDE TABLET, FILM COATED [ST. MARY'S MEDICAL PARK PHARMACY] 1 Current NDC, 1 package rows 20241122_275c0198-10a5-139e-e063-6394a90a72be.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 60760-757-42 60760075742 42 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-757-42) 2024-11-14 No No Current