Home NDC 68788-7382 acyclovir
Product NDC 68788-7382
11-digit product format 687887382
Labeler code 68788
Product ID 68788-7382_54b985ca-0a1e-42f1-b28c-c7685f271859
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form TABLET
Route ORAL
Labeler Preferred Pharmaceuticals Inc.
Application ANDA204314
Marketing category ANDA
Marketing start 2016-08-31
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 2022-12-31
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 68788-7382-2 68788738202 21 TABLET in 1 BOTTLE (68788-7382-2) 21 tablet 2016-08-31 0000-00-00 No No Current 68788-7382-3 68788738203 30 TABLET in 1 BOTTLE (68788-7382-3) 30 tablet 2016-08-31 0000-00-00 No No Current 68788-7382-4 68788738204 40 TABLET in 1 BOTTLE (68788-7382-4) 40 tablet 2016-08-31 0000-00-00 No No Current 68788-7382-5 68788738205 50 TABLET in 1 BOTTLE (68788-7382-5) 50 tablet 2016-08-31 0000-00-00 No No Current 68788-7382-6 68788738206 60 TABLET in 1 BOTTLE (68788-7382-6) 60 tablet 2016-08-31 0000-00-00 No No Current 68788-7382-7 68788738207 28 TABLET in 1 BOTTLE (68788-7382-7) 28 tablet 2016-08-31 0000-00-00 No No Current 68788-7382-8 68788738208 30 TABLET in 1 BOTTLE (68788-7382-8) 30 tablet 2016-08-31 0000-00-00 No No Current