Home NDC 71335-1155
Valacyclovir hydrochloride
Product NDC 71335-1155
11-digit product format 713351155
Labeler code 71335
Product ID 71335-1155_a5f7edc1-cd53-4d40-9760-3446b30ed46f
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Valacyclovir hydrochloride
Dosage form TABLET
Route ORAL
Labeler Bryant Ranch Prepack
Application ANDA077135
Marketing category ANDA
Marketing start 2010-05-24
Marketing end 0000-00-00
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 2023-12-31
Current FDA listing Historical FDA.report record Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71335-1155-1 71335115501 21 TABLET in 1 BOTTLE (71335-1155-1) 21 tablet 2019-03-22 0000-00-00 No No Current