Home NDC 67296-2146 Valacyclovir
Product NDC 67296-2146
11-digit product format 672962146
Labeler code 67296
Product ID 67296-2146_4ca9cf49-74e1-1ef8-e063-6294a90aeae4
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Valacyclovir
Dosage form TABLET
Route ORAL
Labeler Redpharm Drug
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 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 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 67296-2146-1 Valacyclovir 21 in 1 BOTTLE TABLET 21 5 67296-2146-3 Valacyclovir 30 in 1 BOTTLE TABLET 30 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67296-2146 VALACYCLOVIR TABLET [REDPHARM DRUG] 1 Current NDC, 2 package rows 20250410_3251a0f1-cbfd-c9d6-e063-6394a90a09a0.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 67296-2146-1 67296214601 21 TABLET in 1 BOTTLE (67296-2146-1) 21 tablet 2023-02-14 No No Current 67296-2146-3 67296214603 30 TABLET in 1 BOTTLE (67296-2146-3) 30 tablet 2023-02-14 No No Current