Home NDC 50090-2224 Valacyclovir Hydrochloride
Product NDC 50090-2224
11-digit product format 500902224
Labeler code 50090
Product ID 50090-2224_4826c98d-6c86-445f-b808-9df98651628d
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 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 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 50090-2224-0 50090222400 10 TABLET, FILM COATED in 1 BOTTLE (50090-2224-0) 2015-11-09 0000-00-00 No No Current 50090-2224-1 50090222401 14 TABLET, FILM COATED in 1 BOTTLE (50090-2224-1) 2015-11-09 0000-00-00 No No Current 50090-2224-2 50090222402 30 TABLET, FILM COATED in 1 BOTTLE (50090-2224-2) 2015-11-09 0000-00-00 No No Current 50090-2224-3 50090222403 90 TABLET, FILM COATED in 1 BOTTLE (50090-2224-3) 2017-01-04 0000-00-00 No No Current