Home NDC 70934-556 acyclovir
Product NDC 70934-556
11-digit product format 709340556
Labeler code 70934
Product ID 70934-556_f14bb0e9-5cfb-e51b-e053-2995a90ac293
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 2023-01-31
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 0000-00-00
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 70934-556-35 70934055635 35 TABLET in 1 BOTTLE, PLASTIC (70934-556-35) 35 tablet 2020-02-19 0000-00-00 No No Current 70934-556-40 70934055640 40 TABLET in 1 BOTTLE, PLASTIC (70934-556-40) 40 tablet 2020-03-12 0000-00-00 No No Current