Home NDC 50090-2223 Valacyclovir Hydrochloride
Product NDC 50090-2223
11-digit product format 500902223
Labeler code 50090
Product ID 50090-2223_47eaad1f-a29a-4f3a-ba36-a245631171e1
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Valacyclovir Hydrochloride
Dosage form TABLET, FILM COATED
Route ORAL
Labeler A-S Medication Solutions
Application ANDA090682
Marketing category ANDA
Marketing start 2010-05-24
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 2022-12-31
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 50090-2223-0 50090222300 15 TABLET, FILM COATED in 1 BOTTLE (50090-2223-0) 2015-11-09 0000-00-00 No No Current 50090-2223-2 50090222302 30 TABLET, FILM COATED in 1 BOTTLE (50090-2223-2) 2015-11-09 0000-00-00 No No Current 50090-2223-3 50090222303 90 TABLET, FILM COATED in 1 BOTTLE (50090-2223-3) 2015-11-09 0000-00-00 No No Current