Home NDC 60760-469 Valacyclovir
Product NDC 60760-469
11-digit product format 607600469
Labeler code 60760
Product ID 60760-469_bed99bed-3905-5278-e053-2a95a90aeab6
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Valacyclovir
Dosage form TABLET, FILM COATED
Route ORAL
Labeler St. Mary's Medical Park Pharmacy
Application ANDA203047
Marketing category ANDA
Marketing start 2021-03-31
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
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 60760-469-42 Valacyclovir 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 60760-469 VALACYCLOVIR TABLET, FILM COATED [ST. MARY'S MEDICAL PARK PHARMACY] 1 Current NDC, Legacy NDC, 1 package rows 20210406_bed99bed-3904-5278-e053-2a95a90aeab6.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 60760-469-42 60760046942 42 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-469-42) 2021-03-31 0000-00-00 No No Current