Home NDC 68788-7378 acyclovir
Product NDC 68788-7378
11-digit product format 687887378
Labeler code 68788
Product ID 68788-7378_63b72054-7240-4a8b-a655-00c3a6d8a8c5
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form TABLET
Route ORAL
Labeler Preferred Pharmaceuticals Inc.
Application ANDA204314
Marketing category ANDA
Marketing start 2016-08-25
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 Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 68788-7378-2 68788737802 21 TABLET in 1 BOTTLE (68788-7378-2) 21 tablet 2016-08-25 0000-00-00 No No Current 68788-7378-3 68788737803 30 TABLET in 1 BOTTLE (68788-7378-3) 30 tablet 2016-08-25 0000-00-00 No No Current 68788-7378-4 68788737804 40 TABLET in 1 BOTTLE (68788-7378-4) 40 tablet 2016-08-25 0000-00-00 No No Current 68788-7378-5 68788737805 50 TABLET in 1 BOTTLE (68788-7378-5) 50 tablet 2016-08-25 0000-00-00 No No Current 68788-7378-6 68788737806 60 TABLET in 1 BOTTLE (68788-7378-6) 60 tablet 2016-08-25 0000-00-00 No No Current 68788-7378-7 68788737807 25 TABLET in 1 BOTTLE (68788-7378-7) 25 tablet 2016-08-25 0000-00-00 No No Current 68788-7378-8 68788737808 35 TABLET in 1 BOTTLE (68788-7378-8) 35 tablet 2016-08-25 0000-00-00 No No Current