Home NDC 70934-694 acyclovir
Product NDC 70934-694
11-digit product format 709340694
Labeler code 70934
Product ID 70934-694_d672cdb2-6cc2-53ee-e053-2995a90a41a7
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 2020-05-04
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 70934-694-25 70934069425 25 TABLET in 1 BOTTLE, PLASTIC (70934-694-25) 25 tablet 2020-05-04 0000-00-00 No No Current 70934-694-30 70934069430 30 TABLET in 1 BOTTLE, PLASTIC (70934-694-30) 30 tablet 2020-05-06 0000-00-00 No No Current 70934-694-45 70934069445 45 TABLET in 1 BOTTLE, PLASTIC (70934-694-45) 45 tablet 2020-05-04 0000-00-00 No No Current 70934-694-60 70934069460 60 TABLET in 1 BOTTLE, PLASTIC (70934-694-60) 60 tablet 2020-05-08 0000-00-00 No No Current 70934-694-90 70934069490 90 TABLET in 1 BOTTLE, PLASTIC (70934-694-90) 90 tablet 2020-05-14 0000-00-00 No No Current