Home NDC 55700-664 acyclovir
Product NDC 55700-664
11-digit product format 557000664
Labeler code 55700
Product ID 55700-664_9b648c0a-da9f-4d72-a259-471486a4435e
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form TABLET
Route ORAL
Labeler Lake Erie Medical DBA Quality Care Products LLC
Application ANDA204314
Marketing category ANDA
Marketing start 2014-09-10
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 55700-664-15 55700066415 15 TABLET in 1 BOTTLE (55700-664-15) 15 tablet 2019-06-28 0000-00-00 No No Current 55700-664-35 55700066435 35 TABLET in 1 BOTTLE (55700-664-35) 35 tablet 2018-09-14 0000-00-00 No No Current 55700-664-40 55700066440 40 TABLET in 1 BOTTLE (55700-664-40) 40 tablet 2018-07-26 0000-00-00 No No Current 55700-664-60 55700066460 60 TABLET in 1 BOTTLE (55700-664-60) 60 tablet 2018-07-26 0000-00-00 No No Current