Home NDC 70934-557 acyclovir
Product NDC 70934-557
11-digit product format 709340557
Labeler code 70934
Product ID 70934-557_adb61454-c791-3e14-e053-2995a90ae70f
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form TABLET
Route ORAL
Labeler Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Application ANDA077309
Marketing category ANDA
Marketing start 2020-02-19
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 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 70934-557-14 70934055714 14 TABLET in 1 BOTTLE, PLASTIC (70934-557-14) 14 tablet 2020-03-11 0000-00-00 No No Current 70934-557-15 70934055715 15 TABLET in 1 BOTTLE, PLASTIC (70934-557-15) 15 tablet 2020-02-19 0000-00-00 No No Current 70934-557-25 70934055725 25 TABLET in 1 BOTTLE, PLASTIC (70934-557-25) 25 tablet 2020-03-11 0000-00-00 No No Current 70934-557-30 70934055730 30 TABLET in 1 BOTTLE, PLASTIC (70934-557-30) 30 tablet 2020-02-21 0000-00-00 No No Current 70934-557-60 70934055760 60 TABLET in 1 BOTTLE, PLASTIC (70934-557-60) 60 tablet 2020-03-12 0000-00-00 No No Current