Home NDC 63629-6349 Acyclovir
Product NDC 63629-6349
11-digit product format 636296349
Labeler code 63629
Product ID 63629-6349_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 1997-04-30
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 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 63629-6349-1 63629634901 30 TABLET in 1 BOTTLE (63629-6349-1) 30 tablet 2015-09-04 0000-00-00 No No Current 63629-6349-2 63629634902 35 TABLET in 1 BOTTLE (63629-6349-2) 35 tablet 2015-09-28 0000-00-00 No No Current 63629-6349-3 63629634903 50 TABLET in 1 BOTTLE (63629-6349-3) 50 tablet 2016-05-16 0000-00-00 No No Current