Home NDC 70518-2346 valacyclovir hydrochloride
Product NDC 70518-2346
11-digit product format 705182346
Labeler code 70518
Product ID 70518-2346_c846cc3e-13a9-795b-e053-2995a90a74d8
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name valacyclovir hydrochloride
Dosage form TABLET, FILM COATED
Route ORAL
Labeler REMEDYREPACK INC.
Application ANDA201506
Marketing category ANDA
Marketing start 2019-10-04
Marketing end 0000-00-00
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 2022-12-31
Current FDA listing Historical FDA.report record FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 70518-2346-0 70518234600 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2346-0) 2019-10-04 0000-00-00 No No Current 70518-2346-1 70518234601 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2346-1) 2019-10-22 0000-00-00 No No Current 70518-2346-2 70518234602 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2346-2) 2019-11-26 0000-00-00 No No Current