Home NDC 63629-1006 Acyclovir
Product NDC 63629-1006
11-digit product format 636291006
Labeler code 63629
Product ID 63629-1006_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 800 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 63629-1006-1 63629100601 100 TABLET in 1 BOTTLE (63629-1006-1) 100 tablet 2009-10-22 0000-00-00 No No Current 63629-1006-2 63629100602 20 TABLET in 1 BOTTLE (63629-1006-2) 20 tablet 2009-10-22 0000-00-00 No No Current 63629-1006-3 63629100603 300 TABLET in 1 BOTTLE (63629-1006-3) 300 tablet 2009-10-22 0000-00-00 No No Current 63629-1006-4 63629100604 10 TABLET in 1 BOTTLE (63629-1006-4) 10 tablet 2009-10-22 0000-00-00 No No Current 63629-1006-5 63629100605 500 TABLET in 1 BOTTLE (63629-1006-5) 500 tablet 2009-10-22 0000-00-00 No No Current