Home NDC 67296-2127 Valacyclovir Hydrochloride
Product NDC 67296-2127
11-digit product format 672962127
Labeler code 67296
Product ID 67296-2127_4698c788-aa02-6afb-e063-6394a90a708e
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name valacyclovir
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Redpharm Drug
Application ANDA078518
Marketing category ANDA
Marketing start 2010-05-24
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 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 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 67296-2127-2 Valacyclovir Hydrochloride 21 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 21 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67296-2127 VALACYCLOVIR HYDROCHLORIDE (VALACYCLOVIR) TABLET, FILM COATED [REDPHARM DRUG] 2 Current NDC, 1 package rows 20250410_301edb6c-9ce0-f9fa-e063-6294a90a2909.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 67296-2127-2 67296212702 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (67296-2127-2) 2010-05-24 No No Current