Home NDC 68071-5122 Acyclovir
Product NDC 68071-5122
11-digit product format 680715122
Labeler code 68071
Product ID 68071-5122_bbf51aa1-57d8-51a9-e053-2995a90af22a
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form TABLET
Route ORAL
Labeler NuCare Pharmaceuticals,Inc.
Application ANDA074891
Marketing category ANDA
Marketing start 2013-08-08
Marketing end 0000-00-00
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 2022-12-31
Current FDA listing Historical FDA.report record FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 68071-5122-5 68071512205 35 TABLET in 1 BOTTLE (68071-5122-5) 35 tablet 2019-12-05 0000-00-00 No No Current