Home NDC 63629-1005 Acyclovir
Product NDC 63629-1005
11-digit product format 636291005
Labeler code 63629
Product ID 63629-1005_0c77b2dd-bb84-4230-9cd0-81d185f803a0
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form TABLET
Route ORAL
Labeler Bryant Ranch Prepack
Application ANDA075382
Marketing category ANDA
Marketing start 2009-10-22
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 2023-12-31
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 63629-1005-1 63629100501 100 TABLET in 1 BOTTLE (63629-1005-1) 100 tablet 2009-10-22 0000-00-00 No No Current 63629-1005-2 63629100502 25 TABLET in 1 BOTTLE (63629-1005-2) 25 tablet 2009-10-22 0000-00-00 No No Current 63629-1005-3 63629100503 300 TABLET in 1 BOTTLE (63629-1005-3) 300 tablet 2009-10-22 0000-00-00 No No Current 63629-1005-4 63629100504 30 TABLET in 1 BOTTLE (63629-1005-4) 30 tablet 2009-10-22 0000-00-00 No No Current 63629-1005-5 63629100505 500 TABLET in 1 BOTTLE (63629-1005-5) 500 tablet 2009-10-22 0000-00-00 No No Current