Home NDC 63187-627 Valacyclovir hydrochloride
Product NDC 63187-627
11-digit product format 631870627
Labeler code 63187
Product ID 63187-627_55ec9138-f8f7-4222-ad3b-2cf85db6ac28
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Valacyclovir hydrochloride
Dosage form TABLET
Route ORAL
Labeler Proficient Rx LP
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 2020-12-31
Current FDA listing Historical FDA.report record DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63187-627 VALACYCLOVIR HYDROCHLORIDE TABLET [PROFICIENT RX LP] 3 Legacy NDC 20191121_4043f83c-2bb7-4590-b3df-0658f5e627ac.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63187-627-14 63187062714 14 TABLET in 1 BOTTLE (63187-627-14) 14 tablet 2018-12-01 0000-00-00 No No Current 63187-627-28 63187062728 28 TABLET in 1 BOTTLE (63187-627-28) 28 tablet 2018-12-01 0000-00-00 No No Current 63187-627-30 63187062730 30 TABLET in 1 BOTTLE (63187-627-30) 30 tablet 2018-12-01 0000-00-00 No No Current 63187-627-60 63187062760 60 TABLET in 1 BOTTLE (63187-627-60) 60 tablet 2018-12-01 0000-00-00 No No Current 63187-627-90 63187062790 90 TABLET in 1 BOTTLE (63187-627-90) 90 tablet 2018-12-01 0000-00-00 No No Current