Home NDC 70934-512 ACYCLOVIR
Product NDC 70934-512
11-digit product format 709340512
Labeler code 70934
Product ID 70934-512_adcc5c5a-86dc-61af-e053-2995a90ab8c3
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 2020-01-22
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 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 70934-512-30 70934051230 30 TABLET in 1 BOTTLE, PLASTIC (70934-512-30) 30 tablet 2020-01-22 0000-00-00 No No Current 70934-512-45 70934051245 45 TABLET in 1 BOTTLE, PLASTIC (70934-512-45) 45 tablet 2020-01-22 0000-00-00 No No Current 70934-512-60 70934051260 60 TABLET in 1 BOTTLE, PLASTIC (70934-512-60) 60 tablet 2020-01-22 0000-00-00 No No Current