Home NDC 70934-465 ACYCLOVIR
Product NDC 70934-465
11-digit product format 709340465
Labeler code 70934
Product ID 70934-465_a14042bf-5316-11c0-e053-2a95a90aca1b
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name ACYCLOVIR
Dosage form TABLET
Route ORAL
Labeler Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Application ANDA074891
Marketing category ANDA
Marketing start 2019-11-26
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 2021-12-31
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 70934-465-30 70934046530 30 TABLET in 1 BOTTLE, PLASTIC (70934-465-30) 30 tablet 2019-11-26 0000-00-00 No No Current 70934-465-60 70934046560 60 TABLET in 1 BOTTLE, PLASTIC (70934-465-60) 60 tablet 2020-01-08 0000-00-00 No No Current