Home NDC 63629-6376 Acyclovir
Product NDC 63629-6376
11-digit product format 636296376
Labeler code 63629
Product ID 63629-6376_70de6194-dca8-4a3c-828c-395a5b6b45cf
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form TABLET
Route ORAL
Labeler Bryant Ranch Prepack
Application ANDA074556
Marketing category ANDA
Marketing start 1997-04-23
Marketing end 0000-00-00
Substance ACYCLOVIR
Active strength 400 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 Units Marketing start Marketing end Sample Exclude flag Status 63629-6376-1 63629637601 60 TABLET in 1 BOTTLE (63629-6376-1) 60 tablet 2015-09-04 0000-00-00 No No Current 63629-6376-2 63629637602 30 TABLET in 1 BOTTLE (63629-6376-2) 30 tablet 2015-12-29 0000-00-00 No No Current 63629-6376-3 63629637603 50 TABLET in 1 BOTTLE (63629-6376-3) 50 tablet 2017-02-15 0000-00-00 No No Current