Home NDC 68788-7895 acyclovir
Product NDC 68788-7895
11-digit product format 687887895
Labeler code 68788
Product ID 68788-7895_6b95bef0-2722-465c-9593-78aba3ab2106
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form TABLET
Route ORAL
Labeler Preferred Pharmaceuticals Inc.
Application ANDA077309
Marketing category ANDA
Marketing start 2021-04-29
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 2023-12-31
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 68788-7895-2 68788789502 21 TABLET in 1 BOTTLE (68788-7895-2) 21 tablet 2021-04-29 0000-00-00 No No Current 68788-7895-3 68788789503 30 TABLET in 1 BOTTLE (68788-7895-3) 30 tablet 2021-04-29 0000-00-00 No No Current 68788-7895-4 68788789504 40 TABLET in 1 BOTTLE (68788-7895-4) 40 tablet 2021-04-29 0000-00-00 No No Current 68788-7895-5 68788789505 50 TABLET in 1 BOTTLE (68788-7895-5) 50 tablet 2021-04-29 0000-00-00 No No Current