Home NDC 63629-7639 Acyclovir
Product NDC 63629-7639
11-digit product format 636297639
Labeler code 63629
Product ID 63629-7639_9e46e26d-a801-4f36-8422-d868587c9fbd
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 2021-12-31
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 63629-7639-1 63629763901 10 TABLET in 1 BOTTLE (63629-7639-1) 10 tablet 2010-04-05 0000-00-00 No No Current 63629-7639-2 63629763902 20 TABLET in 1 BOTTLE (63629-7639-2) 20 tablet 2010-04-05 0000-00-00 No No Current 63629-7639-3 63629763903 100 TABLET in 1 BOTTLE (63629-7639-3) 100 tablet 2010-04-05 0000-00-00 No No Current 63629-7639-4 63629763904 300 TABLET in 1 BOTTLE (63629-7639-4) 300 tablet 2010-04-05 0000-00-00 No No Current 63629-7639-5 63629763905 500 TABLET in 1 BOTTLE (63629-7639-5) 500 tablet 2010-04-05 0000-00-00 No No Current