Home NDC 63629-7638 Acyclovir
Product NDC 63629-7638
11-digit product format 636297638
Labeler code 63629
Product ID 63629-7638_d28b16b2-6f9f-4121-943e-b07b7841808a
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 2020-12-31
Current FDA listing Historical FDA.report record Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63629-7638-1 63629763801 25 TABLET in 1 BOTTLE (63629-7638-1) 25 tablet 2010-04-05 0000-00-00 No No Current 63629-7638-2 63629763802 30 TABLET in 1 BOTTLE (63629-7638-2) 30 tablet 2010-04-05 0000-00-00 No No Current 63629-7638-3 63629763803 100 TABLET in 1 BOTTLE (63629-7638-3) 100 tablet 2010-04-05 0000-00-00 No No Current 63629-7638-4 63629763804 300 TABLET in 1 BOTTLE (63629-7638-4) 300 tablet 2010-04-05 0000-00-00 No No Current 63629-7638-5 63629763805 500 TABLET in 1 BOTTLE (63629-7638-5) 500 tablet 2010-04-05 0000-00-00 No No Current