Home NDC 63629-7958
Valacyclovir
Product NDC 63629-7958
11-digit product format 636297958
Labeler code 63629
Product ID 63629-7958_9276e10d-668e-4321-81ab-fb4c109e196e
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Valacyclovir
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Bryant Ranch Prepack
Application ANDA203047
Marketing category ANDA
Marketing start 2015-05-25
Marketing end 0000-00-00
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 2023-12-31
Current FDA listing Historical FDA.report record Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 63629-7958-1 63629795801 21 TABLET, FILM COATED in 1 BOTTLE (63629-7958-1) 2021-12-23 0000-00-00 No No Current